Antitumoral derivatives of ET-743

ABSTRACT

Derivatives of Et-743 or Et-770 or Et-729 are provided. The derivatives are of the general formula (Ia) wherein the substituent groups take various permitted meanings.

The present invention relates to derivatives of the ecteinascidins, particularly ecteinascidin743, ET-743.

BACKGROUND OF THE INVENTION

The ecteinascidins such as Et-743 are exceedingly potent antitumor agents isolated from the marine tunicate Ecteinascidia turbinata. Several ecteinascidins have been reported previously in the patent and scientific literature. See, for example:

U.S. Pat. No. 5,256,663, which describes pharmaceutical compositions comprising matter extracted from the tropical marine invertebrate, Ecteinascidia turbinata, and designated therein as ecteinascidins, and the use of such compositions as antibacterial, anti-viral, and/or antitumor agents in mammals.

U.S. Pat. No. 5,089,273, which describes novel compositions of matter extracted from the tropical marine invertebrate, Ecteinascidia turbinata, and designated therein as ecteinascidins 729, 743, 745, 759A, 759B and 770. These compounds are useful as antibacterial and/or antitumor agents in mammals.

U.S. Pat. No. 5,478,932, which describes ecteinascidins isolated from the Caribbean tunicate Ecteinascidia turbinata, which provide in vivo protection against P388 lymphoma, B16 melanoma, M5076 ovarian sarcoma, Lewis lung carcinoma, and the LX-1 human lung and MX-1 human mammary carcinoma xenografts.

U.S. Pat. No. 5,654,426, which describes several ecteinascidins isolated from the Caribbean tunicate Ecteinascidia turbinata, which provide in vivo protection against P388 lymphoma, B16 melanoma, M5076 ovarian sarcoma, Lewis lung carcinoma, and the LX-1 human lung and MX-1 human mammary carcinoma xenografts.

U.S. Pat. No. 5,721,362, which describes a synthetic process for the formation of ecteinascidin compounds and related structures.

U.S. Pat. No. 6,124,293, which relates to semisynthetic ecteinascidins.

WO 9846080, which provides nucleophile substituted and N-oxide ecteinascidins.

WO 9958125, relating to an ecteinascidin metabolite.

WO 0069862, which describes the synthesis of ecteinascidin compounds from cyanosafracin B.

WO 0177115, WO 0187894 and WO 0187895, which describe new synthetic compounds of the ecteinascidin series, their synthesis and biological properties.

See also: Corey, E. J., J. Am. Chem. Soc. 1996, 118, 9202-9203; Rinehart, et al., Journal of National Products 1990, “Bioactive Compounds from Aquatic and Terrestrial Sources”, 53, 771-792; Rinehart et al., Pure and Appl. Chem. 1990, “Biologically active natural products”, 62, 1277-1280; Rinehart, et al., J. Org. Chem. 1990, “Ecteinascidins 729, 743, 745, 759A, 759B, and 770: Potent Antitumor Agents from the Caribbean Tunicate Ecteinascidia turbinata”, 55, 4512-4515; Wright et al., J. Org. Chem. 1990, “Antitumor Tetrahydroisoquinoline Alkaloids from the Colonial Ascidian Ecteinascidia turbinata”, 55, 4508-4512; Sakai et al., Proc. Natl. Acad. Sci. USA 1992, “Additional antitumor ecteinascidins from a Caribbean tunicate: Crystal structures and activities in vivo”, 89, 11456-11460; Science 1994, “Chemical Prospectors Scour the Seas for Promising Drugs”, 266, 1324; Koenig, K. E., “Asymmetric Synthesis”, ed. Morrison, Academic Press, Inc., Orlando, Fla., vol. 5, 1985, pp. 71; Barton, et al., J. Chem Soc. Perkin Trans. I 1982, “Synthesis and Properties of a Series of Sterically Hindered Guandidine Bases”, 2085; Fukuyama et al., J. Am Chem. Soc. 1982, “Stereocontrolled Total Synthesis of (+)-Saframycin B”, 104, 4957; Fukuyama et al., J. Am Chem Soc. 1990, “Total Synthesis of (+)-Saframycin A”, 112, 3712; Saito, et al., J. Org. Chem. 1989, “Synthesis of Saframycins. Preparation of a Key Tricyclic Lactam Intermediate to Saframycin A”, 54, 5391; Still, et al., J. Org. Chem. 1978, “Rapid Chromatographic Technique for Preparative Separations with Moderate Resolution”, 43, 2923; Kofron, W. G.; Baclawski, L. M., J. Org. Chem. 1976, 41, 1879; Guan et al., J. Biomolec. Struc. & Dynam. 1993, 10, 793-817; Shamma et al., “Carbon-13 NMR Shift Assignments of Amines and Alkaloids”, p. 206, 1979; Lown et al., Biochemistry 1982, 21, 419-428; Zmijewski et al., Chem. Biol. Interactions 1985, 52, 361-375; Ito, CRC CRIT. Rev. Anal. Chem. 1986, 17, 65-143; Rinehart et al., “Topics in Pharmaceutical Sciences 1989” pp. 613-626, D. D. Breimer, D. J. A. Cromwelin, K. K. Midha, Eds., Amsterdam Medical Press B. V., Noordwijk, The Netherlands (1989); Rinehart et al., “Biological Mass Spectrometry,” 233-258 eds. Burlingame et al., Elsevier Amsterdam (1990); Guan et al., Jour. Biomolec. Struct. & Dynam. 1993, 10, 793-817; Nakagawa et al., J. Amer. Chem. Soc. 1989, 111: 2721-2722; Lichter et al., “Food and Drugs from the Sea Proceedings” (1972), Marine Technology Society, Washington, D.C. 1973, 117-127; Sakai et al., J. Amer. Chem. Soc. 1996, 118, 9017; Garcia-Rocha et al., Brit. J Cancer 1996, 73: 875-883; Pommier et al., Biochemistry 1996, 35: 13303-13309; Rinehart, K. L. Med. Res. Rev. 2000, 20, 1-27 and Manzanares I. et al. Org. Lett. 2000, 2 (16), 2545-2548; Corey et al., Proc. Natl. Acad. Sci. USA 1999, 96, 3496-3501.

SUMMARY OF THE INVENTION

The present invention is directed to compounds of the general formula Ia.

wherein the substituent groups defined by R₁, R₂, R₄, R₅ are each independently selected of H, C(═O)R′, C(═O)OR′ substituted or unsubstituted C₁-C₁₈ alkyl, substituted or unsubstituted C₂-C₁₈ alkenyl, substituted or

unsubstituted C₂-C₁₈ alkynyl, substituted or unsubstituted aryl;

-   wherein R₆ and R₇ are both ═O and the dotted lines indicate a     quinone ring, or R₆ is —OR₃, where R₃ is H, C(═O)R′, C(═O)OR′     substituted or unsubstituted C₁-C₁₈ alkyl, substituted or     unsubstituted C₂-C₁₈ alkenyl, substituted or unsubstituted C₂-C₁₈     alkynyl, substituted or unsubstituted aryl, R₇ is H, and the dotted     lines indicate a phenyl ring; -   wherein each of the R′ groups is independently selected from the     group consisting of H, OH, NO₂, NH₂, SH, CN, halogen, ═O, C(═O)H,     C(═O)CH₃, CO₂H, substituted or unsubstituted C₁-C₁₈ alkyl,     substituted or unsubstituted C₂-C₁₈ alkenyl, substituted or     unsubstituted C₂-C₁₈ alkynyl, substituted or unsubstituted aryl; -   wherein the substituent groups for X₂, X₃, X₄, X₅, X₆ are     independently selected of H, OH, OR′, SH, SR′, SOR′, SO₂R′, C(═O)R′,     C(═O)OR′, NO₂, NH₂, NHR′, N(R′)₂, NHC(O)R′, CN, halogen, ═O, ′,     substituted or unsubstituted C₁-C₂₄ allyl, substituted or     unsubstituted C₂-C₁₈ alkenyl, substituted or unsubstituted C₂-C₁₈     alkynyl, substituted or unsubstituted aryl, substituted or     unsubstituted heteroaromatic; -   wherein X₁ is independently selected of OR₁, CN, (═O), or H; -   wherein substituent groups for R₁, R₂, R₃, R₄, and R₅ are each     independently selected from the group consisting of H, OH, OR′, SH,     SR′, SOR′, SO₂R′, C(═O)R′, C(═O)OR′, NO₂, NH₂, NHR′, N(R′)₂,     NHC(O)R′, CN, halogen, ═O, substituted or unsubstituted C₁-C₁₈     alkyl, substituted or unsubstituted C₂-C₁₈ alkenyl, substituted or     unsubstituted C₂-C₁₈ alkynyl, substituted or unsubstituted aryl,     substituted or unsubstituted heterocyclic.

More particularly, the invention provides compounds of formula (I):

wherein the substituent groups defined by R₁, R₂, R₄, R₅ are each independently selected of H, C(═O)R′, C(═O)OR′ substituted or unsubstituted C₁-C₁₈ alkyl, substituted or unsubstituted C₂-C₁₈ alkenyl, substituted or unsubstituted C₂-C₁₈ alkynyl, substituted or unsubstituted aryl, or P═O(OR′)₂;

-   where R₃ is H, C(═O)R′, C(═O)OR′ substituted or unsubstituted C₁-C₁₈     alkyl, substituted or unsubstituted C₂-C₁₈ alkenyl, substituted or     unsubstituted C₂-C₁₈ alkynyl, substituted or unsubstituted aryl, R₇     is H, and the dotted lines indicate a phenyl ring; -   wherein each of the R′ groups is independently selected from the     group consisting of H, OH, NO₂, NH₂, SH, CN, halogen, ═O, C(═O)H,     C(═O)CH₃, alkyloxycarbonyl, CO₂H, substituted or unsubstituted     C₁-C₁₈ alkyl, substituted or unsubstituted C₂-C₁₈ alkenyl,     substituted or unsubstituted C₂-C₁₈ alkynyl, substituted or     unsubstituted aryl; -   wherein the substituent groups for X₂, X₃, X₄, X₅ are independently     selected of H, OH, OR′, SH, SR′, SOR′, SO₂R′, C(═O)R′, C(═O)OR′,     NO₂, NH₂, NHR′, N(R′)₂, NHC(O)R′, CN, halogen, ═O, substituted or     unsubstituted C₁-C₁₈ alkyl, substituted or unsubstituted C₂-C₁₈     alkenyl, substituted or unsubstituted C₂-C₁₈ alkynyl, substituted or     unsubstituted aryl, substituted or unsubstituted heteroaromatic; -   wherein X₁ is independently selected of OR₁, CN, (═O), or H; -   wherein substituent groups for R₁, R₂, R₃, R₄, and R₅ are each     independently selected from the group consisting of H, OH, OR′, SH,     SR′, SOR′, SO₂R′, C(═O)R′, C(═O)OR′, NO₂, NH₂, NHR′, N(R′)₂,     NHC(O)R′, CN, halogen, ═O, substituted or unsubstituted C₁-C₁₈     alkyl, substituted or unsubstituted C₂-C₁₈ alkenyl, substituted or     unsubstituted C₂-C₁₈ alkynyl, substituted or unsubstituted aryl,     substituted or unsubstituted heteroaromatic.

In one aspect, the invention provides compounds of formula (I), wherein:

-   R₁, R₃ and R₄ are independently selected from hydrogen, R′, C═OR′,     or COOR′, where R′ is optionally substituted alkyl or alkenyl, the     optional substituents being chosen from halo, amino including amino     derived from amino acid, aryl or heterocyclic; -   R₂ is hydrogen, alkyl or C(═O)OR′, where R′ is alkyl; -   R₅ is hydrogen, alkyl or C(═O)OR′, where R′ is alkylene. -   X₁ is hydrogen, hydroxy, or cyano; -   X₂, X₄ and X₅ are hydrogen; -   X₃ is OR′, where R′ is alkyl; and -   X₆ is hydrogen or alkyl.

Suitable halogen substituents in the compounds of the present invention include F, Cl, Br and I.

Alkyl groups preferably have from 1 to 24 carbon atoms. One more preferred class of alkyl groups has 1 to about 12 carbon atoms, yet more preferably 1 to about 8 carbon atoms, still more preferably 1 to about 6 carbon atoms, and most preferably 1, 2, 3 or 4 carbon atoms. Another more preferred class of alkyl groups has 12 to about 24 carbon atoms, yet more preferably 12 to about 18 carbon atoms, and most preferably 13, 15 or 17 carbon atoms. Methyl, ethyl and propyl including isopropyl are particularly preferred alkyl groups in the compounds of the present invention. As used herein, the term alkyl, unless otherwise modified, refers to both cyclic and noncyclic groups, although cyclic groups will comprise at least three carbon ring members.

Preferred alkenyl and alkynyl groups in the compounds of the present invention have one or more unsaturated linkages and from 2 to about 12 carbon atoms, more preferably 2 to about 8 carbon atoms, still more preferably 2 to about 6 carbon atoms, even more preferably 1, 2, 3 or 4 carbon atoms. The terms alkenyl and alkynyl as used herein refer to both cyclic and noncyclic groups, although straight or branched noncyclic groups are generally more preferred.

Preferred alkoxy groups in the compounds of the present invention include groups having one or more oxygen linkages and from 1 to about 12 carbon atoms, more preferably from 1 to about 8 carbon atoms, and still more preferably 1 to about 6 carbon atoms, and most preferably 1, 2, 3 or 4 carbon atoms.

Preferred alkylthio groups in the compounds of the present invention have one or more thioether linkages and from 1 to about 12 carbon atoms, more preferably from 1 to about 8 carbon atoms, and still more preferably 1 to about 6 carbon atoms. Alkylthio groups having 1, 2, 3 or 4 carbon atoms are particularly preferred.

Preferred alkylsulfinyl groups in the compounds of the present invention include those groups having one or more sulfoxide (SO) groups and from 1 to about 12 carbon atoms, more preferably from 1 to about 8 carbon atoms, and still more preferebly 1 to about 6 carbon atoms. Alkylsulfinyl groups having 1, 2, 3 or 4 carbon atoms are particularly preferred.

Preferred alkylsulfonyl groups in the compounds of the present invention include those groups having one or more sulfonyl (SO₂) groups and from 1 to about 12 carbon atoms, more preferably from 1 to about 8 carbon atoms, and still more preferably 1 to about 6 carbon atoms. Alkylsulfonyl groups having 1, 2, 3 or 4 carbon atoms are particularly preferred.

Preferred aminoalkyl groups include those groups having one or more primary, secondary and/or tertiary amine groups, and from 1 to about 12 carbon atoms, more preferably 1 to about 8 carbon atoms, still more preferably 1 to about 6 carbon atoms, even more preferably 1, 2, 3 or 4 carbon atoms. Secondary and tertiary amine groups are generally more preferred than primary amine moieties.

Suitable heterocyclic groups include heteroaromatic and heteroalicyclic groups. Suitable heteroaromatic groups in the compounds of the present invention contain one, two or three heteroatoms selected from N, O or S atoms and include, e.g., coumarinyl including 8-coumarinyl, quinolinyl including 8-quinolinyl, pyridyl, pyrazinyl, pyrimidyl, furyl, pyrrolyl, thienyl, thiazolyl, oxazolyl, imidazolyl, indolyl, benzofuranyl and benzothiazol. Suitable heteroalicyclic groups in the compounds of the present invention contain one, two or three heteroatoms selected from N, O or S atoms and include, e.g., tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, morpholino and pyrrolindinyl groups.

Suitable carbocyclic aryl groups in the compounds of the present invention include single and multiple ring compounds, including multiple ring compounds that contain separate and/or fused aryl groups. Typical carbocyclic aryl groups contain 1 to 3 separate or fused rings and from 6 to about 18 carbon ring atoms. Specifically preferred carbocyclic aryl groups include phenyl including substituted phenyl such as 2-substituted phenyl, 3-substituted phenyl, 2.3-substituted phenyl, 2,5-substituted phenyl, 2.3.5-substituted and 2.4.5-substituted phenyl, including where one or more of the phenyl substituents is an electron-withdrawing group such as halogen, cyano, nitro, alkanoyl, sulfinyl, sulfonyl and the like; naphthyl including 1-naphthyl and 2-naphthyl; biphenyl; phenanthryl; and anthracyl.

References herein to substituted R′ groups in the compounds of the present invention refer to the specified moiety, typically alkyl or alkenyl, that may be substituted at one or more available positions by one or more suitable groups, e.g., halogen such as fluoro, chloro, bromo and iodo; cyano; hydroxyl; nitro; azido; alkanoyl such as a C1-6 alkanoyl group such as acyl and the like; carboxamido; alkyl groups including those groups having 1 to about 12 carbon atoms or from 1 to about 6 carbon atoms and more preferably 1-3 carbon atoms; alkenyl and alkynyl groups including groups having one or more unsaturated linkages and from 2 to about 12 carbon or from 2 to about 6 carbon atoms; alkoxy groups having those having one or more oxygen linkages and from 1 to about 12 carbon atoms or 1 to about 6 carbon atoms; aryloxy such as phenoxy; alkylthio groups including those moieties having one or more thioether linkages and from 1 to about 12 carbon atoms or from 1 to about 6 carbon atoms; alkylsulfinyl groups including those moieties having one or more sulfinyl linkages and from 1 to about 12 carbon atoms or from 1 to about 6 carbon atoms; alkylsulfonyl groups including those moieties having one or more sulfonyl linkages and from 1 to about 12 carbon atoms or from 1 to about 6 carbon atoms; aminoalkyl groups such as groups having one or more N atoms and from 1 to about 12 carbon atoms or from 1 to about 6 carbon atoms; carbocylic aryl having 6 or more carbons, particularly phenyl (e.g., R being a substituted or unsubstituted biphenyl moiety); and aralkyl such as benzyl; heterocyclic groups including heteroalicyclic and heteroaromatic groups, especially with 5 to 10 ring atoms of which 1 to 4 are heteroatoms, more preferably heterocyclic groups with 5 or 6 ring atoms and 1 or 2 heteratoms or with 10 ring atoms and 1 to 3 heteroatoms.

Preferred R′ groups are present in groups of formula R′, COR′ or OCOR′and include alkyl or alkenyl, that may be substituted at one or more available positions by one or more suitable groups, e.g., halogen such as fluoro, chloro, bromo and iodo, especially ω-chloro or perfluoro; aminoalkyl groups such as groups having one or more N atoms and from 1 to about 12 carbon atoms or from 1 to about 6 carbon atoms, and especially including amino acid, notably glycine, alanine, arginine, asparagine, asparaginic acid, cystein, glutamine, glutamic acid, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine or valine, especially protected forms of such amino acids; carbocylic aryl having 6 or more carbons, particularly phenyl; and aralkyl such as benzyl; heterocyclic groups including heteroalicyclic and heteroaromatic groups, especially with 5 to 10 ring atoms of which 1 to 4 are heteroatoms, more preferably heterocyclic groups with 5 or 6 ring atoms and 1 or 2 heteratoms or with 10 ring atoms and 1 to 3 heteroatoms, the heterocyclic groups optionally being substituted with one or more of the subsitituents permitted for R′ and especially amino such as dimethylamino or with keto.

DESCRIPTION OF PREFERRED EMBODIMENTS

One class of preferred compounds of this invention includes compounds of this invention which have one or more of the following substituents:

-   R₁ is hydrogen; -   alkyl, more preferably alkyl of 1 to 6 carbon atoms; -   C(═O)R′, where R′ is alkyl, more preferably alkyl of 1 to 24 carbon     atoms, especially 1 to 8 or 12 to 18 carbon atoms; haloalkyl, more     preferably ω-chloro- or perfluoro-alkyl of 1 to 4 carbon atoms,     especially ω-chloroethyl or perfluoromethyl, ethyl or propyl;     heterocylicalkyl, more preferably an aylkyl of 1 to 6 carbon atoms     with an ω-heterocyclic substituent suitably having 5 to 10 ring     atoms and 1 to 4 heteroatoms, including fused heteroalicyclic with 3     hetero atoms, such as biotin; aminoalkyl, more preferably alkyl of 1     to 6 carbon atoms, especially 2 carbon atoms, with an ω-amino group     optionally protected for example with alkoxycarbonyl such as     (CH₃)₃C—O—C═O— or other protecting group; -   arylalkylene, especially cinnamoyl; alkylene, especially vinyl or     allyl; aralkyl, such as benzyl; or -   C(═O)OR′, where R′ is alkyl, more preferably alkyl of 1 to 6 carbon     atoms, especially branched alkyl; alkenyl, more preferably allyl; -   R₂ is hydrogen, methyl, or a protecting group including     alkoxycarbonyl such as (CH₃)₃C—O—C═O—. -   R₃ is hydrogen; -   alkyl, more preferably alkyl of 1 to 6 carbon atoms; -   (C═O)R′, where R′ is alkoxy, especially with an alkyl group of 1 to     6 carbon atoms; alkyl, more preferably alkyl of 1 to 24 carbon     atoms, preferably 1 to 8 or 12 to 18 carbon atoms; haloalkyl, more     preferably perfluoroalkyl of 1 to 4 carbon atoms, especially     perfluoromethyl, ethyl or propyl; arylalkylene, especially     cinnamoyl; heterocylicalkyl, more preferably an alkyl of 1 to 6     carbon atoms with an ω heterocyclic substituent suitably having 5 to     12 ring atoms and 1 to 4 heteroatoms, including fused heterocyclic     with 3 ring atoms, such as biotin; heterocyclicalkyl, with     preferably 1 carbon atom in the alkyl group, and more preferably     heteroalicylicmethyl with 5 to 10 ring atoms and 1 to 4 ring atoms,     especially fused heterocylic with 1 to 4 heteroatoms, such as     dimethylaminocoumarin or coumarin; alkylene, especially allyl;     aralkyl, such as benzyl; -   (C═O)OR′, where R′ is alkyl, more preferably alkyl of 1 to 6 carbon     atoms; alkylene, especially vinyl or allyl; aralkyl, such as benzyl. -   R₄ is C(═O)R′, where R′ is alkyl, more preferably alkyl of 1 to 24     carbon atoms, preferably 1 to 8 or 12 to 18 carbon atoms; haloalkyl,     more preferably ω-chloro- or perfluoro-alkyl of 1 to 4 carbon atoms,     especially ω-chloroethyl or perfluoromethyl, ethyl or propyl;     aralkyl, such as benzyl or phenethyl; -   arylalkylene, especially cinnamoyl; aminoalkyl, especially amino     acid, more especially protected amino acid, including protected     cysteinine, notably Fm-S CH₂CH(NHAlloc)-cys or protected alanine,     notably (CH₃)₃C—O—C═O-ala; heterocyclicalkyl, more preferably an     alkyl of 1 to 6 carbon atoms with an ω-heterocyclic substituent     suitably having 5 to 12 ring atoms and 1 to 4 heteroatoms, including     fused heterocyclic with 3 ring atoms, such as biotin; -   heterocyclicalkyl, with preferably 1 carbon atom in the alkyl group,     and more preferably heteroalicyclicmethyl with 5 to 10 ring atoms     and 1 to 4 ring atoms, especially fused heterocylic with 1 to 4     heteroatoms, such as coumarin or dimethylaminocoumarin; -   (C═O)OR′, where R′ is alkyl, more preferably alkyl of 1 to 6 carbon     atoms; -   alkylene, especially vinyl or allyl; aralkyl, such as benzyl; -   P═O(OR′)₂, where R′ is benzyl. -   R₅ is hydrogen; -   alkyl, more preferably alkyl of 1 to 6 carbon atoms; -   (C═O)OR′, where R′ is alkylene, especially vinyl. -   X₁ is hydrogen, hydroxy, or cyano. -   X₂ is hydrogen. -   X₃ is OR′, where R′ is alkyl having 1 to 6 carbon atoms, especially     methyl. -   X₄ is hydrogen. -   X₅ is hydrogen. -   X₆ is hydrogen or alkyl, especially hydrogen or alkyl of 1 to 6     carbon atoms, more especially hydrogen.

Compounds where R₃ is not hydrogen are one class of preferred compounds. In the article by Corey et al., Proc. Natl. Acad. Sci. USA 1999, 96, 3496-3501, a structure-activity relationship is shown for ecteinascidin-type compounds, indicating that a hydrogen is essential. It is stated on page 3498 that “the protection of the other phenolic hydroxyl group on the E subunit resulted in diminished activity”. We find the hydrogen is not essential, see compounds 96, 97 and 98, among many others.

Compounds wherein R₄ is an ester or an ether are among the preferred compounds, for example compounds 57, 60, 61, 63, 65, 68 and 76. In general they have improved toxicology properties and thus give a wider therapeutic window.

In particular, compounds wherein both R₃ and R₄ are not hydrogen are preferred. Of those, compounds with an ester or ether at these positions are most preferred, and in particular esters and carbonates. See compounds 78, 82, 83, 84, 86, 88, 92. Esters with bulky groups (long aliphatic or aromatic residues) give better results. Examples of particularly preferred substituents include octanoic, palmitic, cinnamoyl, hydrocinnamoyl. See compounds 86, 92. Among the carbonates, terButyloxycarbonyl (tBOC) and vinyloxycarbonyl (VOC) are the most preferred substituents for these positions. See ompounds 86 and 92, which are among the best in activity and toxicology. For the ether substituents at these positions, ethyl or a bulky group is preferred.

Compounds with ethyl at R₅, N 2′ are preferred, since there is activity at lower concentrations than those at which the compound begins to be toxic.

Compounds with changes at R₁ are part of this invention, especially ester groups, R₁═R′CO—, with R′ a long aliphatic or aromatic group. See compounds 161, 162, 164, 165, 168, 169, 170, 171, 172, 174, 175. Some of these compounds have substituents at both R₁ and R₃. They have good activity/toxicity properties. For example 170 is active and in heart and myelo non toxic. Compund 174 is very active (E-10) and toxic at higher concentrations (E-8).

There are compounds that have good ADME properties (absorption-distribution-metabolism-excretion) which are good indicative of pharmacokinetics.

As mentioned above, compounds of the present invention, preferably those with bulky substituted groups, have a good therapeutic window and the estherification of the phenols with different acids and carbonates, results in a general enhancement of the pharmaceutical properties: there is a significant decrease in hepatocyte toxicity, and also a good profile on drug-drug interactions since these derivatives do not show cytochrome inhibition having moreover higher metabolic stability.

In a related aspect of this invention, the compounds have one or more of the following features:

R₁ is not acetyl. Preferably it has at least 4, 5 or 6 carbon atoms, for example up to 18 or 24 carbon atoms. Suitable substituents include esters COR′, where R′ is alkyl, alkenyl, often with one or more substituents. Alkyl, substituted alkyl, alkenyl and arylalkenyl are preferred, with suitable substituents including aryl, heterocyclic. Other defintions for R1 include esters of formula COR′ derived from an amino acid, optionally a protected amino acid.

R₃ is not hydrogen. Preferably it is R′, COR′ or COOR′ where R′ is a substituent with some bulk. Such bulky substituents include those with branched chain groups, unsaturated groups or cyclic groups including aromatic groups. Thus, branched alkyl, cycloalkyl, branched alkenyl, aryl, heteroaromatic and related groups are preferred for inclusion within the structure of the substituent R₃. Preferably the total number of carbon atoms in R₃ is 2 to 24, more preferably 6 to 18 carbon atoms. Typically R₃ is an ester, ether or carbonate, being of formula COR′, R′ or COOR′.

R₄ is not hydrogen. Preferably it is R′, COR′ or COOR′ where R′ is a substituent with some bulk. Such bulky substituents include those with branched chain groups, unsaturated groups or cyclic groups including aromatic groups. Thus, branched alkyl, cycloalkyl, branched alkenyl, aryl, heteroaromatic and related groups are preferred for inclusion within the structure of the substituent R₄. Preferably the total number of carbon atoms in R₄ is 2 to 24, more preferably 6 to 18 carbon atoms. Typically R₄ is an ester, ether or carbonate, being of formula COR′, R′ or COOR′.

Examples of protecting groups for amino and other substituents are given in WO 0069862, and we expressly incorporate that disclosure.

Without being exhaustive, another class of preferred compounds of this invention have one or more of the following definitions:

-   X₁ is H, —CN or —OH, most especially —OH or —CN. -   X₂ is hydrogen. -   X₃ is methoxy. -   X₄ and X₅ are hydrogen. -   R₁ is preferably H or acetyl; arylalkyl, especially benzyl;     alkyl-CO— (alkyl being up to 25 carbon atoms, such as up to 17, 19     or 21 carbon atoms and preferably an odd number of carbon atoms     corresponding to a fatty acid carboxylic acid of even number of     carbon atoms or else a low number of carbon atoms such as 1 to 6)     especially CH₃—(CH₂)_(n)—CO— where n is for example 1.2.4.6.12.14 or     16; haloalkyl-CO—, especially trifluoromethylcarbonyl;     arylalkyl-CO—, especially benzyl-CO—; arylalkenyl-CO—, especially     cinnamoyl-CO—; most especially R₁ is H, acetyl or cinnamoyl. -   R₂ is H; alkyl, especially methyl; alkyl-O—CO—, especially     t-butyl-O—CO— or alkenyl-O—CO—, especially allyl-O—CO—. -   R₃ is preferably H or acetyl; alkyl (alkyl being 1 to 6 carbon     atoms), especially C₁ to C₃ alkyl; alkenyl, especially allyl;     arylalkyl, especially benzyl; alkyl-CO— (alkyl being up to 25 carbon     atoms, such as up to 17, 19 or 21 carbon atoms and preferably an odd     number of carbon atoms corresponding to a fatty acid carboxylic acid     of even number of carbon atoms or else a low number of carbon atoms     such as 1 to 6) especially CH₃—(CH₂)_(n)—CO— where n is for example     1.2.4.6.12.14 or 16 and derivatives thereof, as in     Biotin-(CH₂)₄—CO—; -   arylalkenyl-CO—, especially cinnamoyl-CO—; alkyl-O—CO—, especially     t-butyl-O—CO—; arylalkyl-O—CO—, especially benzyl-O—CO—;     alkenyl-O—CO, especially allyl-O—CO—. -   R₄ is preferably H, acetyl, alkyl (alkyl being 1 to 6 carbon atoms)     especially C₁ to C₃ alkyl; alkenyl, especially allyl; arylalkyl,     especialy benzyl; alkyl-CO— (alkyl being up to 25 carbon atoms, such     as up to 17, 19 or 21 carbon atoms and preferably an odd number of     carbon atoms corresponding to a fatty acid carboxylic acid of even     number of carbon atoms or else a low number of carbon atoms such as     1 to 6) especially CH₃—(CH₂)_(n)—CO— where n is for example     1.2.4.6.12.14 or 16 and derivatives thereof, as in     Biotin-(CH₂)₄—CO—; -   haloalkyl-CO—, especially trifluoromethylcarbonyl; amino acid acyl     or a derivative thereof, as in FmSCH₂CH(NHAlloc)CO—;     arylalkenyl-CO—, especially cinnamoyl-CO—; alkyl-O—CO—, especially     tert-butyl-O—CO—; alkenyl-O—CO—, especially allyl-O—CO;     arylalkyl-O—CO—, especially benzyl-O—CO—; protecting group as in     PO(OBn)₂; most especially R₄ is H, acyl y cinnamoyl. -   R₅ is H or alkyl (alkyl being 1 to 6 carbon atoms) and R₅ is most     especially H or C₁ to C₃ alkyl.

This application claims priority of a British patent application. We expressly incorporate by reference any disclosure which is in the specification of that British priority application and which is not in the present application.

Furthermore, we expressly incorporate by reference each of WO 0069862, WO 0177115, WO 0187894 and WO 0187895 for their discussion of substituents which correspond to the substituents of the present invention. Any definitions given in any of these earlier applications for a particular substituent can be adopted for a substituent of a compound of this invention.

Furthermore, we do not claim any of the compounds disclosed in the earlier applications, and we expressly disclaim any such compounds. We expressly incorporate by reference each of the earlier applications for the wording of any disclaimer which might be necessary.

In one aspect, this invention is concerend with a derivative of Et-743 or Et-770 or Et-729 which differs in one or more of the following aspects:

-   R₁ is not acetyl, and in particular is a group which is not COR′     where R′ is hydrogen, methyl or ethyl, or which is not COR′ where R′     is hydrogen, methyl, ethyl or propyl. -   R₁ is not R′ where R′ is methyl or ethyl, or where R′ is methyl,     ethyl or propyl or where R′ is methyl, ethyl, propyl or butyl. -   R₂ is not methyl. -   R₆ is R₃ and is not hydrogen. -   R₄ is not hydrogen. -   R₅ is not hydrogen. -   R₆ and R₇ are ═O. -   X₁ is not hydroxy or cyano.

In one aspect, this invention provides a derivative wherein:

-   R₁ is not acetyl, and in particular is a group which is not COR′     where R′ is hydrogen, methyl or ethyl, or which is not COR′ where R′     is hydrogen, methyl, ethyl or propyl; R₁ is not R′ where R′ is     methyl or ethyl, or where R′is methyl, ethyl or propyl or where R′     is methyl, ethyl, propyl or butyl; and R₆ is R₃ and is not hydrogen.

In a further aspect, this invention provides a derivative wherein:

-   R₁ is not acetyl, and in particular is a group which is not COR′     where R′ is hydrogen, methyl or ethyl, or which is not COR′ where R′     is hydrogen, methyl, ethyl or propyl; R₁ is not R′ where R′ is     methyl or ethyl, or where R′is methyl, ethyl or propyl or where R′     is methyl, ethyl, propyl or butyl; and R₄ is not hydrogen.

In a related aspect, this invention provides a derivative wherein:

-   R₆ is R₃ and is not hydrogen; and R₄ is not hydrogen.

In yet another aspect, this invention provides a derivative wherein:

-   R₁ is not acetyl, and in particular is a group which is not COR′     where R′ is hydrogen, methyl or ethyl, or which is not COR′ where R′     is hydrogen, methyl, ethyl or propyl; R₁ is not R′ where R′ is     methyl or ethyl, or where R′is methyl, ethyl or propyl or where R′     is methyl, ethyl, propyl or butyl; R₆ is R₃ and is not hydrogen; R₄     is not hydrogen.

The compounds of the present invention can be prepared synthetically from the intermediate compound 15 described in the U.S. Pat. No. 5,721,362, ET-770 and ET-729. Numerous active antitumoral compounds have been prepared from this compound and it is believed that many more compounds can be formed in accordance with the teachings of the present disclosure.

Antitumoral activities of these compounds include leukaemias, lung cancer, colon cancer, kidney cancer, prostate cancer, ovarian cancer, breast cancer, sarcomas and melanomas.

Another especially preferred embodiment of the present invention is pharmaceutical compositions useful as antitumor agents which contain as active ingredient a compound or compounds of the invention, as well as the processes for their preparation.

Examples of pharmaceutical compositions include any solid (tablets, pills, capsules, granules etc.) or liquid (solutions, suspensions or emulsions) with suitable composition or oral, topical or parenteral administration.

Administration of the compounds or compositions of the present invention may be any suitable method, such as intravenous infusion, oral preparation, intraperitoneal and intravenous preparation.

Administration of the compounds or compositions of the present invention may be by any suitable method, such as intravenous infusion, oral preparations, intraperitoneal and intravenous administration. We prefer that infusion times of up to 24 hours are used, more preferably 2-12 hours, with 2-6 hours most preferred. Short infusion times which allow treatment to be carried out without an overnight stay in hospital are especially desirable. However, infusion may be 12 to 24 hours or even longer if required. Infusion may be carried out at suitable intervals of say 2 to 4 weeks. Pharmaceutical compositions containing compounds of the invention may be delivered by liposome or nanosphere encapsulation, in sustained release formulations or by other standard delivery means.

The correct dosage of the compounds will vary according to the particular formulation, the mode of application, and the particular situs, host and tumour being treated. Other factors like age, body weight, sex, diet, time of administration, rate of excretion, condition of the host, drug combinations, reaction sensitivities and severity of the disease shall be taken into account. Administration can be carried out continuously or periodically within the maximum tolerated dose.

The compounds and compositions of this invention may be used with other drugs to provide a combination therapy. The other drugs may form part of the same composition, or be provided as a separate composition for administration at the same time or a different time. The identity of the other drug is not particularly limited, and suitable candidates include:

-   a) drugs with antimitotic effects, especially those which target     cytoskeletal elements, including microtubule modulators such as     taxane drugs (such as taxol, paclitaxel, taxotere, docetaxel),     podophylotoxins or vinca alkaloids (vincristine, vinblastine); -   b) antimetabolite drugs such as 5-fluorouracil, cytarabine,     gemcitabine, purine analogues such as pentostatin, methotrexate); -   c) alkylating agents such as nitrogen mustards (such as     cyclophosphamide or ifosphamide); -   d) drugs which target DNA such as the antracycline drugs adriamycin,     doxorubicin, pharmorubicin or epirubicin; -   e) drugs which target topoisomerases such as etoposide; -   f) hormones and hormone agonists or antagonists such as estrogens,     antiestrogens (tamoxifen and related compounds) and androgens,     flutamide, leuprorelin, goserelin, cyprotrone or octreotide; -   g) drugs which target signal transduction in tumour cells including     antibody derivatives such as herceptin; -   h) alkylating drugs such as platinum drugs (cis-platin,     carbonplatin, oxaliplatin, paraplatin) or nitrosoureas; -   i) drugs potentially affecting metastasis of tumours such as matrix     metalloproteinase inhibitors; -   j) gene therapy and antisense agents; -   k) antibody therapeutics; -   l) other bioactive compounds of marine origin, notably the didemnins     such as aplidine; -   m) steroid analogues, in particular dexamethasone; -   n) anti-inflammatory drugs, in particular dexamethasone; and -   o) anti-emetic drugs, in particular dexamethasone.

Examples of biological activities of the compounds of the present invention are included in tables I, II and III at the end of the document.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The preferred methods of producing the compounds are described below in schemes I-VI.

Scheme I includes acylation reactions through the different procedures described in the experimental part. Compound 1 corresponds to Et-770. Starting from this compound it is possible to obtain target compounds following acylation methods: A ((RCO)₂O/base), B (RCOCl/base), C (RCOOH/DMAP/EDC.HCl) and D (ROCOCl/base). Other acylation reactions have been performed from compound 25 which belongs to the family of the structures of formula I and compound 47 whose structure is described further.

Compounds 29, 30, 31, 32 and 33 are compounds wherein R₁, R₂ and R₃ is a vinyl radical or an hydrogen atom.

In Scheme II method E involves reactions of alkylation (RBr/CS₂CO₃) and method G (RCHO/NaBCNBH₃/AcOH) is the reductive alkylation at N-2′. Compounds 34, 35 and 36 are obtained when the alkylation reaction is performed with MeI. With these methodologies we generate N and O-alkyl derivatives starting from compound 1. In compound 53 a phosphate group is introduced at position C-6′ using dibenzyl phosphite.

Scheme III includes hydrolysis of tert-butylcarbonate in C-6′ through method F (TFA/H₂O/CH₂Cl₂) and hydrolysis of acetyl groups in C-5 from compound 42 with KOH/H₂O/THF and in C-6′ from compound 6 with TEA/MeOH/THF. Also is described the formation of compound 52 starting from compound 1 through an oxidation reaction of the right aromatic ring.

The different analogs of Et-743 wherein R₁, R₂ and R₃ are acyl, carbonate, carbamate or alkyl groups are prepared following method H (AgNO₃/CH₃CN/H₂O) or I (CuBr/THF/H₂O) from the derivatives of Et-770 (Scheme IV). In both cases the reaction involves the transformation of the nitrile group in C-21 into the hydroxyl group. Other specific derivatives as compounds 96, 97, 98, 99, 100, 101 and 102 are synthetised from their corresponding analogs of Et-770, compounds 51, 47, 36, 31, 32, 52 and 48 following the same methodology.

In Scheme V the starting material is compound 106 obtained from compound 4 by hydrolysis of the acetyl group in C-5 with KOH/THF/H₂O. From compound 106 and by esterification and alkylation reactions can be prepared derivatives with structures of formula I. The next step includes the hydrolysis of the tert-butylcarbonate group (method F: TFA/H₂O/CH₂Cl₂ or method J: TMSCl, NaI; CH₃CN/H₂O) to afford derivatives of structures of formula III which are transformed into the final compounds (structure of formula IV) by conversion of the nitrile group in C-21 into the hydroxyl group. This last step is achieved following method H (AgNO₃/CH₃CN/H₂O), method I (CuBr/THF/H₂O) or method K (CuCl/THF/H₂O). In the case of derivatives of structure of formula I wherein R₁ and R₂ are Boc, R₁ are Boc, AlaBoc and Voc radicals the hydrolysis of the tert-butylcarbonyl involves also the hydrolysis of these ester functionalities. These compounds are transformed into the final analogs through method H.

From Et-729 it is possible to obtain target compounds through different experimental conditions. In the attempts to prepare compound 186, other two compounds (184 and 185) were isolated as it is described in the scheme VI. Treatment of compound 186 with Alloc chloroformiate, pyridine and DMAP affords compound 187. With Boc anhydride with o whithout DIPEA we are able to obtain Boc derivatives (compounds 188, 189 and 190). From compound 190 through an alkylation reaction (CS₂CO₃, allyl bromide) is prepared compound 199 which is transformed into compound 201 by hydrolysis of tert-butyl carbonate groups following method F.

From the key compound 188 through esterification reactions it is possible to generate compounds of structure of formula I mono or di sustitued. Hydrolisis of tert-butyl carbonate group (method F) and transformation of the nitrile group in C-21 into the hydroxyl group (method H) lead to the compounds of structure of fromula III. Also from compound 188 by a reductive methylation it is obtained compound 200 with a methyl group in position N-2′. Hydrolisis of the amide bond (method F) and conversion of the nitrile group into the hydroxyl group (method H) affords compound 217.

In this scheme compound 221 can be obtained from compound 218, described in the Patent WO 01/77115 A1 as compound 24, following a transamination reaction to afford 219 and a Pictect-Spengler cyclization to give compound 220. Final step is the conversion of nitrile group into OH in C-21 with the usual methodology (method K) using AgNO₃. Also compound 224 can be obtained from compound 222, described in the WO 00/69862 as compound 36, following a Pictect-Splenger cyclization to give compound 223. Final step is the conversion of nitrile group into OH in C-21 with the usual methodology (method K)

Experimental Part

Method A: To a solution of 1 equiv. of ET-770 (1) in CH₂Cl₂ (0.032M) under Argon were added 2 equiv. of the anhydride and 2 equiv. of pyridine. The reaction was followed by TLC and quenched with NaHCO₃, extracted with CH₂Cl₂ and the organic layers dried over Na₂SO₄. Flash chromatography gives pure compounds.

EXAMPLE 1

2. ¹H-RMN (300 MHz, CDCl₃): δ 6.60 (s, 1H); 6.59 (s, 1H); 6.56 (s, 1H); 6.00 (dd, 2H); 5.73 (s, 1H); 5.01 (d, 1H); 4.55 (s, 1H); 4.32 (s, 1H); 4.27 (d, 1H); 4.17 (d, 1H); 4.11 (dd, 1H); 3.78 (s, 3H); 3.55 (s, 3H); 3.51 (d, 1H); 3.42 (s, 1H); 3.16-3.06 (m, 1H); 2.94-2.92 (m, 2H); 2.81-2.75 (m, 1H); 2.64-2.58 (m, 1H); 2.51-2.44 (m, 1H); 2.35-2.12 (m, 2H); 2.31 (s, 3H); 2.26 (s, 3H); 2.23 (s, 3H); 2.19 (s, 3H); 2.03 (s, 3H).

¹³C-RMN (75 MHz, CDCl₃): δ 172.1, 168.9, 168.1, 148.4, 147.8, 145.3, 143.0, 141.3, 140.1, 138.5, 132.5, 130.8, 129.3, 128.7, 122.4, 121.0, 120.7, 118.1, 118.0, 114.0, 111.8, 102.0, 101.8, 64.8, 61.1, 60.3, 60.1, 59.5, 55.1, 54.7, 53.3, 42.3, 41.9, 41.6, 39.5, 29.6, 28.6, 24.1, 20.5, 20.3, 15.7, 9.6.

ESI-MS m/z: Calcd for C₄₂H₄₄N₄O₁₀S: 812.3 Found (M+H⁺): 813.3

EXAMPLE 2

3. ¹H-RMN (300 MHz, CDCl₃): δ 6.48 (s, 1H); 6.47 (s, 1H); 6.44 (s, 1H); 6.01 (dd, 2H); 5.70 (s, 1H); 5.50 (s, 1H); 4.70-4.78 (m, 2H); 4.39 (s, 1H); 4.24 (dd, 1H); 4.12-4.08 (m, 2H); 3.80 (s, 3H); 3.59 (s, 3H); 3.55 (d, 1H); 3.42-3.39 (m, 1H); 3.22 (d, 1H); 2.90 (d, 2H); 2.65 (t, 2H); 2.51 (d, 1H); 2.32 (s, 3H); 2.27-2.03 (m, 2H); 2.40 (s, 3H); 2.12 (s, 3H); 2.03 (s, 3H).

¹³C-RMN (75 MHz, CDCl₃): δ 168.5, 167.6, 147.3, 145.4, 145.2, 143.1, 141.8, 140.7, 130.8, 129.7, 127.0, 126.3, 125.3, 122.5, 121.4, 118.5, 117.8, 114.3, 114.0, 113.8, 109.5, 102.1, 71.4, 62.2, 61.0, 60.3, 60.2, 60.1, 55.3, 55.1, 54.9, 42.6, 41.9, 39.0, 31.7, 29.3, 24.8, 22.8, 20.5, 15.7, 14.2, 9.9.

ESI-MS m/z: Calcd for C₄₂H₄₁F₃N₄O₁₁S: 867.2 Found (M+H⁺): 866.2

EXAMPLE 3

4. ¹H-RMN (300 MHz, CDCl₃): δ6.68 (s.1H); 6.58 (s, 1H); 6.57 (s, 1H); 6.00 (dd, 2H); 5.74 (s, 1H); 5.00 (d, 1H); 4.54 (s, 1H); 4.31 (s, 1H); 4.26 (dd, 1H); 4.17 (d 1H); 4.11 (dd, 1H); 3.78 (s, 3H); 3.58 (s, 3H); 3.51 (d, 1H); 3.42-3.40 (m, 1H); 3.14-3.06 (m, 1H); 2.94-2.92 (m, 2H); 2.81-2.75 (m, 1H); 2.64-2.58 (m, 1H); 2.51-2.44 (m, 1H); 2.35-2.21 (m, 2H); 2.31 (s, 3H); 2.26 (s, 3H); 2.19 (s, 3H); 2.03 (s, 3H); 1.50 (s, 9H).

¹³C-RMN (75 MHz, CDCl₃): δ 172.0, 168.0, 151.5, 148.5, 147.8, 145.3, 143.0, 141.2, 140.0, 138.8, 132.4, 130.7, 129.2, 128.6, 122.1, 122.0, 120.6, 118.1, 118.0, 113.9, 111.9, 101.8, 83.3, 64.7, 61.0, 60.2, 60.0, 59.6, 59.5, 55.2, 54.6, 54.5, 42.2, 41.8, 41.5, 39.5, 28.6, 27.5, 24.1, 20.3, 15.7, 9.6.

ESI-MS m/z: Calcd for C₄₅H₅₀N₄O₁₂S: 870.3 Found (M+H⁺): 871.3

5: ¹H-RMN (300 MHz, CDCl₃): δ 6.92 (s, 1H); 6.69 (s, 1H); 6.55 (s, 1H); 6.00 (dd, 2H); 5.73 (s, 1H); 5.00 (d, 1H); 4.44 (s, 1H); 4.32 (s, 1H); 4.18 (d, 1H); 4.09 (dd, 1H); 3.93 (d, 1H); 3.79 (s, 3H); 3.58 (s, 3H); 3.53 (d, 1H); 3.46-3.44 (m, 1H); 3.12-3.04 (m, 1H); 2.97 (d, 2H); 2.83-2.77 (m, 1H); 2.65-2.58 (m, 1H); 2.51-2.46 (m, 1H); 2.32-2.03 (m, 2H); 2.32 (s, 3H); 2.31 (s, 3H); 2.17 (s, 3H); 2.04 (s, 3H); 1.53 (s, 9H); 1.50 (s, 9H).

¹³C-RMN (75 MHz, CDCl₃): δ 172.0, 168.4, 151.5, 151.2, 148.5, 148.1, 145.6, 144.0, 141.3, 140.1, 138.9, 132.3, 131.3, 130.3, 128.7, 126.9, 124.3, 122.2, 121.0, 117.8, 113.8, 111.8, 101.9, 83.4, 83.2, 64.9, 61.1, 60.0, 59.9, 59.6, 59.1, 55.6, 55.2, 54.4, 42.2, 41.9, 41.5, 39.5, 28.6, 27.6, 27.5, 23.9, 20.1, 15.7, 9.6.

ESI-MS m/z: Calcd for C₅₀H₅₈N₄O₁₄S: 970.1 Found (M+H⁺): 971.3

EXAMPLE 4

Compound 6 is obtained with 45 equiv of Ac₂O and 113 equiv. of pyridine and catalytic amount of DMAP.

6. ¹H-NMR (300 MHz, CDCl₃): δ 6.95 (s, 1H), 6.62 (s, 1H), 6.54 (s, 1H), 6.02 (dd, 2H), 5.01 (d, 1H), 4.44 (bs, 1H), 4.32 (s, 1H), 4.19 (d, 1H), 4.12 (dd, 1H), 3.82 (d, 1H), 3.77 (s, 3H), 3.65 (s, 3H), 3.53 (bd, 1H), 3.47-3.43 (m, 1H), 3.14-3.05 (m, 1H), 3.00-2.97 (m, 2H), 2.86-2.78 (m, 1H), 2.69-2.58 (m, 1H), 2.52-2.44 (m, 1H), 2.38-2.15 (m, 2H), 2.38 (s, 3H), 2.32 (s, 3H), 2.30 (s, 3H), 2.24 (s, 3H), 2.15 (s, 3H), 2.04 (s, 3H).

ESI-MS m/z: Calcd for C₄₄H₄₆N₄O₁₂S: 854.3 Found (M+H⁺): 855.3

EXAMPLE 5

Method B: To a solution of 1 equiv. of Et-770 (1) in CH₂Cl₂ (0.032M) under Argon at room temperature were added 2 equiv. of base and 2 equiv. of the acid chloride. The reaction was followed by TLC and quenched with NaHCO₃, extracted with CH₂Cl₂ and the organic layers dried with Na₂SO₄. Flash chromatography gives pure compounds.

After chromatographic purification 25% of starting material was recuperated.

7. ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 2H); 6.56 (s, 1H); 6.00 (dd, 2H); 5.74 (s, 1H); 5.01 (d, 1H); 4.55 (s, 1H); 4.32 (s, 1H); 4.27 (dd, 1H); 4.17 (d, 1H); 4.11 (dd, 1H); 3.78 (s, 3H); 3.54 (s, 3H); 3.51 (d, 1H); 3.42 (s, 1H); 3.16-3.05 (m, 1H); 2.94-2.93 (m, 2H); 2.81-2.75 (m, 1H); 2.64-2.58 (m, 1H); 2.51-2.44 (m, 1H); 2.48 (t, 2H); 2.35-2.11 (m, 2H); 2.31 (s, 3H); 2.26 (s, 3H); 2.19 (s, 3H); 2.03 (s, 3H); 1.73 (m, 2H); 1.00 (t, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.1, 168.9, 168.1, 148.4, 147.8, 145.3, 143.0, 141.3, 140.1, 132.4, 130.8, 129.3, 128.6, 122.4, 121.0, 120.7, 118.1, 114.0, 111.7, 107.2, 101.8, 64.8, 61.0, 60.3, 60.0, 59.6, 59.5, 55.1, 54.7, 54.6, 42.3, 41.9, 41.6, 39.5, 35.8, 33.7, 29.6, 28.6, 24.1, 20.3, 18.5, 15.7, 14.0, 9.6.

ESI-MS m/z: Calcd. for C₄₄H₄₈N₄O₁₁S: 840.3 Found (M+H⁺): 841.3.

EXAMPLE 6

After chromatographic purification 28% of starting material was recuperated.

8. ¹H-NMR (300 MHz, CDCl₃): δ 7.80 (d, 1H); 7.56-7.54 (m, 2H); 7.41-7.39 (m, 3H); 6.69 (s, 1H); 6.60 (s, 2H); 6.59 (d, 1H); 6.00 (dd, 2H); 5.74 (s, 1H); 5.03 (d, 1H); 4.56 (s, 1H); 4.33 (s, 1H); 4.28 (dd, 1H); 4.17 (d, 1H); 4.11 (dd, 1H); 3.79 (s, 3H); 3.58 (s, 3H); 3.52 (d, 1H); 3.42-3.40 (m, 1H); 3.16-3.06 (m, 1H); 2.96-2.93 (m, 2H); 2.82-2.75 (m, 1H); 2.64-2.59 (m, 1H); 2.54-2.46 (m, 1H); 2.38-2.12 (m, 2H); 2.32 (s, 3H); 2.28 (s, 3H); 2.20 (s, 3H); 2.04 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.1, 169.0, 148.4, 147.8, 145.3, 143.0, 141.3, 140.1, 138.5, 132.5, 130.8, 129.3, 128.9, 128.6, 127.4, 127.3, 122.4, 121.0, 120.7, 118.1, 114.0, 111.7, 101.8, 64.8, 61.1, 60.3, 60.1, 59.6, 59.5, 55.1 54.7, 54.6, 42.3, 41.9, 41.6, 39.5, 29.7, 28.6, 24.1, 20.6, 20.4, 15.8, 9.7.

ESI-MS m/z: Calcd. for C₄₉H₄₈N₄O₁₁S: 900.3 Found (M+H⁺): 901.3

EXAMPLE 7

9 was obtained using 10 equiv. of butyryl chloride and 10 equiv. of TEA.

¹H-NMR (300 MHz, CDCl₃): 6.95 (s, 1H); 6.60 (s, 1H); 6.54 (s, 1H); 6.01 (dd, 2H); 5.01 (d, 1H); 4.45 (s, 1H); 4.32 (s, 1H); 4.17 (d, 1H); 4.09 (dd, 1H); 3.80 (d, 1H); 3.75 (s, 3H); 3.54 (s, 3H); 3.51 (d, 1H); 3.44 (s, 1H); 3.16-3.05 (m, 1H); 2.99-2.97 (m, 2H); 2.85-2.79 (m, 1H); 2.64-2.58 (m, 1H); 2.61 (t, 2H); 2.51-2.44 (m, 1H); 2.48 (t, 2H); 2.33-2.02 (m, 2H); 2.32 (s, 3H); 2.29 (s, 3H); 2.15 (s, 3H); 2.04 (s, 3H); 1.86 (m, 2H); 1.73 (m, 2H); 1.09 (t, 3H); 1.00 (t, 3H).

ESI-MS m/z: Calcd. for C₄₈H₅₄N₄O₁₂S: 910.3 Found (M+H⁺): 911.3.

EXAMPLE 8

10. ¹H-NMR (300 MHz, CDCl₃): δ 7.94 (d, 1H); 7.81 (d, 1H); 7.63-7.54 (m, 4H); 7.46-7.39 (m, 6H); 6.99 (s, 1H); 6.70 (s, 1H); 6.66 (d, 1H); 6.60 (d, 1H); 6.59 (s, 1H); 6.02 (dd, 2H); 5.04 (d; 1H); 4.55 (s, 1H); 4.35 (s, 1H); 4.21 (d, 1H); 4.13 (dd, 1H); 3.92 (d, 1H); 3.79 (s, 3H); 3.57 (s, 3H); 3.54 (d, 1H); 3.48-3.45 (m, 1H); 3.20-3.10 (m, 1H); 3.01-2.99 (m, 2H); 2.88-2.80 (m, 1H); 2.74.2.62 (m, 1H); 2.56-2.50 (m, 1H); 2.41-2.15 (m, 2H); 2.35 (s, 3H); 2.34 (s, 3H); 2.19 (s, 3H); 2.06 (s, 3H).

ESI-MS m/z: Calcd. for C₅₈H₅₄N₄O₁₂S: 1030.3 Found (M+H⁺): 1031.3.

EXAMPLE 9

The reaction was performed using 4 equiv. of hydrocynamoyl chloride and 2 equiv. of pyridine. After chromatographic purification 25% of starting material was recuperated.

11. ¹H-NMR (300 MHz, CDCl₃): δ 7.31-7.20 (m, 5H); 6.59 (s, 1H); 6.55 (s, 1H); 6.53 (s, 1H); 6.03 (s, 1H); 5.97 (s, 1H); 5.76 (s, 1H); 5.01 (d, 1H); 4.56 (s, 1H); 4.32 (s, 1H); 4.28 (d, 1H); 4.17 (d, 1H); 4.11 (dd, 1H); 3.78 (s, 3H); 3.56-3.50 (m, 1H); 3.51 (s, 3H); 3.42 (s, 1H); 3.14-2.92 (m, 3H); 3.02 (t, 2H); 2.87-2.78 (m, 1H); 2.83 (t, 2H); 2.67-2.43 (m, 4H); 2.3.2.25 (m, 1H); 2.31 (s, 3H); 2.27 (s, 3H); 2.19 (s, 3H); 2.03 (s, 3H).

¹³C-RMN (75 MHz, CDCl₃): δ 172.2, 171.2, 148.6, 148.0, 145.5, 143.2, 141.5, 140.4, 140.3, 138.7, 132.6, 131.0, 129.6, 128.8, 128.7, 128.6, 128.5, 126.5, 122.6, 121.2, 120.9, 118.3, 118.2, 114.2, 111.9, 102.1, 65.0, 61.3, 60.5, 60.3, 59.8, 59.7, 55.3, 54.8, 54.7, 42.3, 42.1, 41.8, 39.6, 35.6, 35.5, 31.4, 30.9, 29.9, 28.6, 24.3, 20.6, 16.0, 9.9.

ESI-MS m/z: Calcd. for C₄₉H₅₀N₄O₁₁S: 902.3 Found (M+H⁺): 903.2.

EXAMPLE 10

12. ¹H-NMR (300 MHz, CDCl₃): δ6.68 (s, 1H); 6.58 (s, 1H); 6.47 (s, 1H); 6.06 (d, 1H); 5.97 (d, 1H); 5.02 (d, 1H); 4.59 (s, 1H); 4.37 (s, 1H); 4.29 (d, 1H); 4.19-4.16 (m, 2H); 3.85 (s, 2H); 3.75 (s, 3H); 3.55 (s, 3H); 3.53 (s, 1H); 3.43 (d, 1H); 3.07-2.80 (m, 5H); 3.00 (t, 2H); 2.83 (t, 2H); 2.61-2.57 (m, 1H); 2.44-2.33 (m, 1H); 2.37 (m, 3H); 2.29 (s, 3H); 2.21 (s, 3H); 2.03 (s; 3H).

ESI-MS m/z: Calcd. for C₄₃H₄₅ClN₄O₁₁S: 860.2 Found (M+H⁺): 861.3.

EXAMPLE 11

13. ¹H-NMR (300 MHz, CDCl₃): δ6.69 (s, 1H); 6.63 (s, 1H); 6.59 (s, 1H); 6.04 (s, 1H); 5.96 (s, 1H); 5.74 (s, 1H); 5.02 (d, 1H); 4.58 (s, 1H); 4.33 (s, 1H); 4.28 (d, 1H); 4.18 (d, 1H); 4.13 (dd, 1H); 3.78 (s, 3H); 3.57 (s, 3H); 3.51 (d, 1H); 3.42 (s, 1H); 3.14-3.06 (m, 1H); 2.94 (d, 2H); 2.82-2.76 (m, 1H); 2.69-2.59 (m, 1H); 2.54-2.48 (m, 1H); 2.36-2.14 (m, 1H); 2.32 (s, 3H); 2.26 (s, 3H); 2.19 (s, 3H); 2.03 (s, 3H).

ESI-MS m/z: Calcd. for C₄₄H₄₁F₇N₄O₁₁S: 966.2 Found (M+H⁺): 967.3.

EXAMPLE 12

Method C: To a solution of 1 equiv. of ET-770 (1) in CH₂Cl₂ (0.032M) under Argon were added 2 equiv. of acid, 2 equiv. of DMAP and 2 equiv. of EDC.HCl. The reaction was stirred at room temperature for 2 h. After this time was diluted with CH₂Cl₂, washed with brine and the organic layer dried with Na₂SO₄. Flash chromatography gives pure compounds.

14. ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 2H); 6.56 (s, 1H); 6.00 (dd, 2H); 5.72 (s, 1H); 5.01 (d, 1H); 4.55 (s, 1H); 4.32 (s, 1H); 4.27 (dd, 1H); 4.17 (d 1H); 4.10 (dd, 1H); 3.79 (s, 3H); 3.54 (s, 3H); 3.51 (d, 1H); 3.42 (s, 1H); 3.16-3.05 (m, 1H); 2.94-2.93 (m, 2H); 2.81-2.75 (m, 1H); 2.64-2.58 (m, 1H); 2.51-2.44 (m, 1H); 2.49 (t, 2H); 2.35-2.11 (m, 2H); 2.32 (s, 3H); 2.27 (s, 3H); 2.19 (s, 3H); 2.03 (s, 3H); 1.73-1.68 (m, 2H); 1.25-1.15 (m, 8H); 1.02 (t, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.1, 171.8, 148.4, 147.8, 145.3, 143.0, 141.3, 140.1, 138.6, 132.4, 130.8, 129.3, 128.6, 122.9, 122.4, 121.0, 120.7, 120.6, 118.1, 114.0, 111.7, 101.8, 64.8, 61.0, 60.3, 60.0, 59.6, 59.5, 55.1, 54.7, 54.6, 42.3, 41.8, 41.5, 39.5, 33.9, 33.7, 31.9, 31.6, 30.1, 29.3, 28.9, 28.8, 28.6, 26.9, 24.9, 24.1, 22.6, 22.5, 20.3, 15.7, 14.0, 9.6.

ESI-MS m/z: Calcd. for C₄₈H₅₆N₄O₁₁S: 896.3 Found (M+H⁺): 897.3.

EXAMPLE 13

Compound 15 is obtained following method C, using 10 equiv. of octanoic acid and 10 equiv. of EDC.HCl and 10 equiv. of DMAP):

15. ¹H-NMR (300 MHz, CDCl₃): δ 6.94 (s, 1H); 6.59 (s, 1H); 6.53 (s, 1H); 6.01 (dd, 2H); 5.01 (d, 1H); 4.45 (s, 1H); 4.32 (s, 1H); 4.18 (d, 1H); 4.10 (dd, 1H); 3.80 (d, 1H); 3.74 (s, 3H); 3.54 (s, 3H); 3.51 (d, 1H); 3.44 (s, 1H); 3.16-3.05 (m, 1H); 2.99-2.97 (m, 2H); 2.88-2.79 (m, 1H); 2.64-2.58 (m, 1H); 2.61 (t, 2H); 2.51-2.44 (m, 1H); 2.49 (t, 2H); 2.35-2.15 (m, 2H); 2.32 (s, 3H); 2.29 (s, 3H); 2.15 (s, 3H); 2.03 (s, 3H); 1.88-1.78 (m, 2H); 1.74-1.56 (m, 4H); 1.39-1.24 (m, 20H).

¹³C-NMR (75 MHz, CDCl₃): δ 182.1, 172.2, 172.0 171.4, 148.7, 148.2, 145.7, 143.9, 141.5, 140.4, 138.9, 132.3, 131.7, 130.8, 128.8, 127.4, 124.6, 122.8, 121.0, 118.0, 114.1, 111.9, 102.2, 65.1, 61.3, 60.3, 60.2, 59.8, 59.4, 56.1, 55.3, 54.6, 42.6, 42.3, 41.8, 39.7, 34.4, 34.1, 33.8, 31.8, 29.9, 29.4, 29.2, 29.1, 29.0, 28.7, 25.4, 25.2, 24.9, 24.2, 22.7, 20.5, 16.0, 14.2, 9.8.

ESI-MS m/z: Calcd. for C₅₆H₇₀N₄O₁₂S: 1022.4 Found (M+H⁺): 1023.5.

EXAMPLE 14

Compounds 16 and 17 were obtained using Method C.

16: ¹H-NMR (300 MHz, CDCl₃): δ 6.61 (s, 2H); 6.56 (s, 1H); 6.00 (dd, 2H); 5.75 (s, 1H); 5.01 (d, 1H); 4.56 (s, 1H); 4.32 (s, 1H); 4.27 (dd, 1H); 4.17 (d, 1H); 4.09 (dd, 1H); 3.79 (s, 3H); 3.53 (s, 3H); 3.50 (d, 1H); 3.41 (s, 1H); 3.16-3.05 (m, 1H); 2.95-2.93 (m, 2H); 2.81-2.75 (m, 1H); 2.68-2.55 (m, 1H); 2.51-2.44 (m, 1H); 2.49 (t, 2H); 2.39-2.11 (m, 2H); 2.32 (s, 3H); 2.28 (s, 3H); 2.19 (s, 3H); 2.03 (s, 3H); 1.73-1.64 (m, 2H); 1.40-1.17 (m, 27H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 171.8, 168.0, 148.4, 147.8, 145.3, 143.0, 141.3, 140.1, 138.6, 132.3, 130.8, 129.8, 129.3, 128.6, 122.4, 121.0, 120.7, 118.0, 114.0, 111.7, 101.8, 64.8, 61.0, 60.2, 60.0, 59.6, 59.5, 55.1, 54.6, 54.6, 42.2, 41.8, 41.5, 39.5, 33.9, 31.8, 29.7, 29.63, 29.60, 29.44, 29.30, 29.21, 29.07, 28.9, 28.5, 24.9, 24.1, 22.6, 20.3, 15.7, 14.0, 9.6.

ESI-MS m/z: Calcd. for C₅₆H₇₂N₄O₁₁S: 1008.4 Found (M+H⁺): 1009.5.

17: ¹H-NMR (300 MHz, CDCl₃): δ 6.94 (s, 1H); 6.59 (s, 1H); 6.54 (s, 1H); 6.02 (dd, 2H); 5.01 (d, 1H); 4.45 (s, 1H); 4.33 (s, 1H); 4.18 (d 1H); 4.10 (dd, 1H); 3.79 (d, 1H); 3.75 (s, 3H); 3.54 (s, 3H); 3.52 (d, 1H); 3.49 (s, 1H); 3.15-3.05 (m, 1H); 2.99-2.97 (m, 2H); 2.83-2.75 (m, 1H); 2.68-2.55 (m, 1H); 2.62 (t, 2H); 2.51-2.44 (m, 1H); 2.49 (t, 2H); 2.36-2.11 (m, 2H); 2.32 (s, 3H); 2.29 (s, 3H); 2.16 (s, 3H); 2.04 (s, 3H); 1.86-1.78 (m, 2H); 1.72-1.75 (m, 2H); 1.40-1.10 (m, 54H).

ESI-MS m/z: Calcd. for C₇₂H₁₀₂N₄O₁₂S: 1246.7 Found (M+H⁺): 1247.6.

EXAMPLE 15

Compound 18 is obtained with 1.5 equiv. of acid, 2.5 equiv. of DMAP and 2.5 equiv. of EDC.HCl (Method C)

18 ¹H-NMR (300 MHz, CDCl₃): δ 7.74 (d, 2H), 7.64 (t, 2H), 7.38 (t, 2H), 7.31-7.27 (m, 2H), 6.60 (s, 1H), 6.57 (s, 1H), 6.55 (s, 1H), 5.98 (d, 2H), 5.96-5.83 (m, 1H), 5.72 (s, 1H), 5.58 (d, 1H), 5.37-5.18 (m, 2H), 5.04 (d, 1H), 4.88-4.79 (m, 1H), 4.58 (bd, 3H), 4.32 (s, 1H), 4.25 (d, 1H), 4.18 (d, 1H), 4.12-4.08 (m, 2H), 3.79 (s, 3H), 3.51 (d, 1H), 3.45 (s, 3H), 3.45-3.42 (m, 1H), 3.16-3.11 (m, 5H), 2.95-2.93 (m, 2H), 2.82-2.75 (m, 1H), 2.63-2.50 (m, 1H), 2.46-2.41 (m, 1H), 2.32-2.13 (m, 2H), 2.32 (s, 3H), 2.27 (s, 3H), 2.20 (s, 3H), 2.03 (s, 3H).

ESI-MS m/z: Calcd. for C₆₁H₆₁N₅O₁₃S₂: 1135.4 Found (M+H⁺): 1136.3.

EXAMPLE 16

A mixture of compopunds 19 and 20 were obtained with 1.5 equiv. of biotin, 2.5 equiv. of DMAP and 2.5 equiv. of EDC.HCl. (Method C)

19: ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 2H), 6.56 (s, 1H), 6.00 (d, 2H), 5.81 (bs, 1H), 5.26 (bs, 1H), 5.02 (d, 1H), 4.83 (bs, 1H), 4.57 (bs, 3H), 4.51-4.47 (m, 1H), 4.33-4.29 (m, 3H), 4.18 (d, 1H), 4.14-4.11 (m, 1H), 3.79 (s, 3H), 3.55 (s, 3H), 3.52-3.50 (m, 1H), 3.49-3.42 (m, 1H), 3.19-3.13 (m, 2H), 2.94-2.87 (m, 3H), 2.78-2.70 (m, 2H), 2.62-2.48 (m, 4H), 2.38-2.16 (m, 2H), 2.32 (s, 3H), 2.27 (s, 3H), 2.20 (s, 3H), 2.03 (s, 3H), 1.79-1.50 (m, 6H).

ESI-MS m/z: Calcd. for C₅₀H₅₆N₆O₁₂S₂: 996.3 Found (M+H⁺): 997.3.

20: ¹H-NMR (300 MHz, CDCl₃): δ 6.95 (s, 1H), 6.62 (s, 1H), 6.52 (bs, 1H), 6.01 (d, 2H), 5.57 (bs, 1H), 5.40 (bs, 1H), 5.01 (d, 1H), 4.99 (bs, 1H), 4.92 (bs, 1H), 4.51-4.28 (m, 6H), 4.18 (d, 1H), 4.13-4.09 (m, 1H), 3.80-3.77 (m, 4H), 3.55 (s, 3H), 3.55-3.52 (m, 1H), 3.46-3.42 (m, 1H), 3.24-3.12 (m, 3H), 3.02-2.52 (m, 13H), 2.33-2.15 (m, 2H), 2.33 (s, 6H), 2.15 (s, 3H), 2.05 (s, 3H), 1.87-1.47 (m, 12H).

ESI-MS m/z: Calcd. for C₆₀H₇₀N₈O₁₄S₃: 1222.4 Found (M+H⁺): 1223.3.

EXAMPLE 17

21. Was obtained using Method C

¹H-NMR (300 MHz, CDCl₃): δ 8.66 (s, 1H); 7.66-7.59 (m, 2H); 7.35-7.29 (m, 2H); 6.74 (s, 1H); 6.60 (s, 1H); 6.59 (s, 1H); 6.01 (d, 1H); 5.94 (d, 1H); 5.81 (s, 1H); 5.02 (d, 1H); 4.55 (s, 1H); 4.31 (s, 1H); 4.26 (d, 1H); 4.18 (d, 1H); 4.13-4.06 (m, 2H); 3.77 (s, 3H); 3.55 (s, 3H); 3.50 (d, 1H); 3.41 (s, 1H); 3.15-3.06 (m, 1H); 2.94 (d, 2H); 2.80-2.75 (m, 1H); 2.68-2.58 (m, 1H); 2.52-2.47 (m, 1H); 2.37-2.11 (m, 1H); 2.31 (s, 3H); 2.26 (s, 3H); 2.18 (s, 3H); 2.02 (s, 3H).

ESI-MS m/z: Calcd. for C₅₀H₄₆N₄O₁₃S: 942.8 Found (M+Na⁺): 965.1.

EXAMPLE 18

Compounds 22 and 23 are obtained using Method C as a mixture 3:1 and described together in ¹H-RMN.

22, 23. ¹H-NMR (300 MHz, CDCl₃): δ 7.46 (d, 1H); 7. 43 (d, 1H); 6.89 (s, 1H); 6.64-6.34 (m, 9H); 6.19 (s, 1H); 6.18 (s, 1H); 6.03 (s, 1H); 6.02 (d, 1H); 5.97 (d, 1H); 5.95 (d, 1H); 5.80 (s, 1H); 5.01 (d, 1H); 4.99 (d, 1H); 4.55 (s, 2H); 4.30 (s, 2H); 4.27-4.23 (m 2H); 4.19-4.15 (m, 2H); 4.10 (dd, 1H); 4.09 (dd, 1H); 4.01-3.90 (m, 2H); 3.85 (s, 4H); 3.77 (s, 6H); 3.68 (s, 2H); 3.59 (s, 1H); 3.56-3.46 (m, 2H); 3.49 (s, 6H); 3.40 (s, 2H); 3.13-3.06 (m, 2H); 3.04 (s, 12H); 2.96 (s, 6H); 2.92 (d, 4H); 2.81-2.73 (m, 2H); 2.63-2.56 (m, 2H); 2.49-2.41 (m, 2H); 2.30 (s, 3H); 2.28 (s, 3H); 2.25 (s, 3H); 2.18 (s, 3H); 2.10 (s, 3H); 2.09 (s, 3H); 2.02 (s, 3H); 2.01 (s, 3H).

ESI-MS m/z: Calcd. for C₅₃H₅₃N₅O₁₃S (22) 1000.08 and Calcd. for C₆₆H₆₄N₆O₁₆S (23) 1229.3. Found (M⁺): 1000.2 (22) and 1229.2 (23).

EXAMPLE 19

24 was obtained using Method C.

¹H-NMR (300 MHz, CDCl₃): δ 6.61 (s, 1H), 6.58 (s, 1H), 6.56 (s, 1H), 5.98 (d, 2H), 5.84 (s, 1H), 5.09 (bd, 1H), 5.00 (d, 1H), 4.54-4.51 (m, 2H), 4.31 (s, 1H), 4.27 (d, 1H), 4.17 (d, 1H), 4.12-4.07 (m, 1H), 3.77 (s, 3H), 3.53 (s, 3H), 3.50 (d, 1H), 3.42-3.39 (m, 1H), 3.13-3.04 (m, 1H), 2.94-2.92 (m, 2H), 2.79-2.75 (m, 1H), 2.66-2.56 (m, 1H), 2.50-2.45 (m, 1H), 2.35-2.02 (m, 2H), 2.31 (s, 3H), 2.26 (s, 3H), 2.18 (s, 3H), 2.02 (s, 3H), 1.48 (d, 3H), 1.43 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 171.5, 168.1, 154.9, 148.1, 147.8, 145.3, 142.9, 141.2, 140.0, 138.2, 132.7, 130.7, 129.3, 128.6, 122.2, 120.9, 120.6, 118.0, 113.9, 113.3, 111.7, 101.8, 79.8, 64.8, 61.0, 60.2, 60.1, 59.5, 59.5, 55.1, 54.6, 54.5, 42.1, 41.8, 41.5, 39.4, 28.5, 28.2, 24.1, 20.4, 18.7, 15.7, 9.6.

ESI-MS m/z: Calcd. for C₄₈H₅₅N₅O₁₃S: 941.3 Found (M+H⁺): 942.3.

EXAMPLE 20

Method D: To a solution of 1 equiv. of starting material in CH₂Cl₂ (0.032M) under Argon were added 2 equiv. of chloroformiate and 2 equiv. of base and the mixture was stirred at room temperature. The reaction was followed by TLC and quenched with NaHCO₃, extracted with CH₂Cl₂ and the organic layers dried with Na₂SO₄. Flash chromatography gives pure compounds.

The reaction is performed with 3.3 equiv. of Alloc chloride and 3.3 equiv. of pyridine.

25. ¹H-NMR (300 MHz, CDCl₃): δ 6.70 (s, 1H), 6.59 (s, 1H), 6.57 (s, 1H), 6.07-5.89 (m, 1H), 6.00 (d, 2H), 5.76 (s, 1H), 5.42-5.27 (m, 2H), 5.01 (d, 1H), 4.69-4.66 (m, 2H), 4.56 (bs, 1H), 4.33 (s, 1H), 4.27 (d, 1H), 4.17 (d, 1H), 4.01 (dd, 1H), 3.79 (s, 3H), 3.58 (s, 3H), 3.51 (bd, 1H), 3.45-3.40 (m, 1H), 3.16-3.06 (m, 1H), 2.97-2.91 (m, 2H), 2.85-2.75 (m, 1H), 2.70-2.57 (m, 1H), 2.53-2.45 (m, 1H), 2.37-2.12 (m, 2H), 2.32 (s, 3H), 2.27 (s, 3H), 2.20 (s, 3H), 2.04 (s, 3H).

ESI-MS m/z: Calcd. for C₄₄H₄₆N₄O₁₂S: 854.3 Found (M+H⁺): 855.0.

EXAMPLE 21

The reaction was performed with excess of Alloc Chloride and pyridine and catalytic DMAP (method D). Some starting material was recovered after chromatographic purification.

26. ¹H-NMR (300 MHz, CDCl₃): δ 6.96 (s, 1H), 6.70 (s, 1H), 6.56 (s, 1H), 6.06-5.89 (m, 2H), 6.01 (d, 2H), 5.44-5.27 (m, 4H), 5.00 (d, 1H), 4.82-4.67 (m, 4H), 4.47 (bs, 1H), 4.34 (s, 1H), 4.19-4.09 (m, 2H), 3.94 (d, 1H), 3.79 (s, 3H), 3.57 (s, 3H), 3.54-3.45 (m, 2H), 3.15-3.03 (m, 1H), 2.99-2.97 (m, 2H), 2.84-2.77 (m, 1H), 2.70-2.59 (m, 1H), 2.53-2.44 (m, 1H), 2.32-2.17 (m, 8H), 2.17 (s, 3H), 2.05 (s, 3H).

ESI-MS m/z: Calcd. for C₄₈H₅₀N₄O₁₄S: 938.3 Found (M+H⁺): 939.3.

EXAMPLE 22

The reaction was performed with 3.0 equiv. of pyridine (Method D).

27. ¹H-NMR (300 MHz, CDCl₃): δ 7.38-7.33 (m, 5H); 6.69 (s, 1H); 6.59 (s, 1H); 6.57 (s, 1H); 5.99 (dd, 2H); 5.75 (s, 1H); 5.21 (s, 2H); 5.00 (d, 1H); 4.56 (s, 1H); 4.32 (s, 1H); 4.27 (dd, 1H); 4.17 (d, 1H); 4.10 (dd, 1H); 3.78 (s, 3H); 3.54 (s, 3H); 3.51 (d, 1H); 3.41 (s, 1H); 3.16-3.06 (m, 1H); 2.94-2.93 (m, 2H); 2.81-2.75 (m, 1H); 2.68-2.58 (m, 1H); 2.49-2.44 (m, 1H); 2.35-2.13 (m, 2H); 2.31 (s, 3H); 2.26 (s, 3H); 2.19 (s, 3H); 2.03 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 168.1, 148.4, 147.8, 145.3, 143.0, 141.3, 140.1, 138.9, 134.9, 132.8, 130.7, 129.3, 128.7, 128.5, 128.3, 121.9, 121.0, 120.7, 118.0, 114.0, 111.9, 101.8, 70.2, 64.8, 61.0, 60.3, 60.1, 59.6, 59.5, 55.1, 54.7, 54.6, 42.2, 41.8, 41.5, 39.5, 29.6, 28.6, 24.1, 20.3, 15.7, 9.6.

ESI-MS m/z: Calcd. for C₄₈H₄₈N₄O₁₂S: 904.3 Found (M+H⁺): 905.3.

EXAMPLE 23

28: Was obtained following Method C using TEA as base.

¹H-NMR (300 MHz, CDCl₃): δ 7.40-7.34 (m, 10H); 6.95 (s, 1H); 6.69 (s, 1H); 6.54 (s, 1H); 5.99 (dd, 2H); 5.33 (d, 1H); 5.23 (s, 1H); 5.21 (s, 2H); 5.00 (d, 1H); 4.43 (s, 1H); 4.32 (s, 1H); 4.17 (d, 1H); 4.10 (dd, 1H); 3.90 (d, 1H); 3.75 (s, 3H); 3.53 (s, 3H); 3.50 (d, 1H); 3.44 (s, 1H); 3.20-3.01 (m, 1H); 2.97-2.96 (m, 2H); 2.82-2.75 (m, 1H); 2.68-2.56 (m, 1H); 2.51-2.42 (m, 1H); 2.28-2.00 (m, 2H); 2.31 (s, 3H); 2.19 (s, 3H); 2.12 (s.3H); 2.03 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.2, 168.7, 153.4, 153.1, 148.6, 148.2, 145.7, 144.3, 141.5, 140.4, 139.1, 135.1, 132.8, 131.7, 130.8, 129.0, 128.9, 128.8, 128.7, 128.5, 128.4, 127.5, 124.5, 122.4, 122.2, 121.1, 117.9, 114.0, 113.6, 112.1, 102.1, 70.7, 70.5, 65.2, 61.3, 60.4, 60.2, 59.8, 59.4, 55.7, 55.3, 54.6, 42.4, 42.1, 41.7, 39.7, 28.8, 24.1, 20.2, 15.9, 9.8.

ESI-MS m/z: Calcd. for C₅₆H₅₄N₄O₁₄S: 1038.3 Found (M+H⁺): 1039.8.

EXAMPLE 24

29. was obtained using Method D.

¹H-NMR (300 MHz, CDCl₃): δ 7.08 (dd, 1H); 6.72 (s, 1H); 6.60 (s, 1H); 6.59 (s, 1H); 6.03 (s, 1H); 5.96 (s, 1H); 5.77 (s, 1H); 5.01 (d, 1H); 4.99 (dd, 1H); 4.63 (dd, 1H); 4.56 (s, 1H); 4.32 (s, 1H); 4.27 (d, 1H); 4.17 (d, 1H); 4.11 (dd, 1H); 3.78 (s, 3H); 3.58 (s, 3H); 3.51 (d, 1H); 3.42 (s, 1H); 3.15-3.06 (m, 1H); 2.93 (d, 2H); 2.82-2.75 (m, 1H); 2.68-2.57 (m, 1H); 2.52-2.46 (m, 1H); 2.36-2.14 (m, 1H); 2.31 (s, 3H); 2.26 (s, 3H); 2.19 (s, 3H); 2.02 (s, 3H).

ESI-MS m/z: Calcd. for C₄₃H₄₄N₄O₁₂S: 840.2 Found (M+H⁺): 841.3.

EXAMPLE 25

The reaction was performed with 5.0 equiv. of TEA and 10 equiv. of vinylchloroformiate (method D).

30: ¹H-NMR (300 MHz, CDCl₃): δ 7.14 (dd, 1H); 7.08 (dd, 1H); 6.99 (s, 1H); 6.73 (s, 1H); 6.58 (s, 1H); 6.04 (d, 1H); 5.97 (d, 1H); 5.03-4.97 (m, 2H); 4.70 (dd, 1H); 4.63 (dd, 1H); 4.48 (s, 1H); 4.33 (s, 1H); 4.17 (d, 1H); 4.13 (dd, 1H); 3.95 (d, 1H); 3.80 (s, 3H); 3.59 (s, 3H); 3.54 (d, 1H); 3.46 (s, 1H); 3.13-3.05 (m, 1H); 2.99 (d, 2H); 2.88-2.77 (m, 1H); 2.70-2.59 (m, 1H); 2.52-2.46 (m, 1H); 2.27-2.12 (m, 2H); 2.35 (s, 3H); 2.33 (s, 3H); 2.17 (s, 3H); 2.05 (s, 3H).

ESI-MS m/z: Calcd. for C₄₆H₄₆N₄O₁₄S: 910.2 Found (M+H⁺): 911.2.

31: ¹H-NMR (300 MHz, CDCl₃): δ 7.17 (dd, 1H); 7.07 (dd, 1H); 7.02 (dd, 1H); 6.86 (s, 1H); 6.74 (s, 1H); 6.33 (s, 1H); 6.07 (d, 1H); 5.95 (d, 1H); 5.01 (dd, 1H); 4.99 (dd, 1H); 4.83 (d, 1H); 4.75 (dd, 1H); 4.68 (dd, 1H); 4.65 (dd, 1H); 4.51 (s, 1H); 4.43 (dd, 1H); 4.35 (s, 1H); 4.12 (d, 1H); 4.05 (dd, 1H); 3.92 (d, 1H); 3.83 (s, 3H); 3.56 (s, 3H); 3.52 (d, 1H); 3.46-3.44 (m, 1H); 3.34 (d, 1H); 3.02-2.88 (m, 2H); 2.77-2.66 (m, 1H); 2.52-2.27 (m, 3H); 2.41 (s, 3H); 2.23 (s, 3H); 2.14 (s, 3H); 2.04 (s, 3H).

ESI-MS m/z: Calcd. for C₄₉H₄₈N₄O₁₆S: 980.2 Found (M+Na⁺): 1003.2.

EXAMPLE 26

32: ¹H-NMR (300 MHz, CDCl₃): δ 7.07 (dd, 1H); 7.01 (dd, 1H); 6.72 (s, 1H); 6.47 (s, 1H); 6.35 (s, 1H); 6.06 (s, 1H); 5.94 (s, 1H); 5.74 (s, 1H); 5.00 (dd, 1H); 4.84 (d, 1H); 4.72 (d, 1H); 4.65 (dd, 1H); 4.62 (s, 1H); 4.41 (dd, 1H); 4.34 (s, 1H); 4.25 (d, 1H); 4.15-3.99 (m, 3H); 3.80 (s, 3H); 3.55 (s, 3H); 3.51-3.27 (m, 3H); 2.96-2.82 (m, 2H); 2.77-2.66 (m, 1H); 2.54-2.44 (m, 3H); 2.33 (s, 3H); 2.21 (s, 3H); 2.16 (s, 3H); 2.01 (s, 3H).

ESI-MS m/z: Calcd. for C₄₆H₄₆N₄O₁₄S: 910.2 Found (M+H⁺): 911.2.

33: ¹H-NMR (300 MHz, CDCl₃): δ 7.02 (dd, 1H); 6.46 (s, 1H); 6.46 (s, 1H); 6.17 (s, 1H); 6.06 (d, 1H); 5.95 (d, 1H); 5.75 (s, 1H); 5.47 (s, 1H); 4.82 (d, 1H); 4.72 (d, 1H); 4.62 (s, 1H); 4.40 (dd, 1H); 4.33 (s, 1H); 4.25 (d, 1H); 4.11 (d, 1H); 4.01 (dd, 1H); 4.03-3.96 (m, 1H); 3.80 (s, 3H); 3.59 (s, 3H); 3.51-3.38 (m, 3H); 3.22 (d, 1H); 2.96-2.82 (m, 2H); 2.72-2.62 (m, 1H); 2.52-2.40 (m, 2H); 2.33 (s, 3H); 2.28-2.18 (m, 1H); 2.22 (s, 3H); 2.16 (s, 3H); 2.03 (s, 3H).

ESI-MS m/z: Calcd. for C₄₃H₄₄N₄O₁₂S: 840.2 Found (M+Na⁺): 863.2.

EXAMPLE 27

Method E: To a solution of 1 equiv. of Et-770 (1), or compound 4 in DMF (0.032M) under Argon at room temperature were added 2 equiv. of CS₂CO₃ and 2 equiv. of the allyl halide. The reaction was followed by TLC and quenched with NaHCO₃, extracted with CH₂Cl₂ and the organic layers dried with Na₂SO₄. Flash chromatography gives pure compounds.

This mixture of compounds is obtained with 1.5 equiv. of MeI and 1.0 equiv. of CS₂CO₃. After chromatographic purification is recovered 21% of starting material and a fraction of the mixture of the three compounds.

34: ¹H-NMR (300 MHz, CDCl₃): δ d 6.60 (s, 1H), 6.48 (s, 1H), 6.40 (s, 1H), 6.01 (d, 2H), 5.72 (s, 1H), 5.02 (d, 1H), 4.57 (bp, 1H), 4.34 (s, 1H), 4.28 (d, 1H), 4.18 (d, 1H), 4.13-4.11 (m, 1H), 3.80 (s, 3H), 3.76 (s, 3H), 3.61 (s, 3H), 3.51 (d, 1H), 3.44-3.41 (m, 1H), 3.17-3.10 (m, 1H), 2.95-2.94 (m, 2H), 2.82-2.78 (m, 1H), 2.70-2.62 (m, 1H), 2.52-2.47 (m, 1H), 2.38-2.04 (m, 2H), 2.33 (s, 3H), 2.26 (s, 3H), 2.20 (s, 3H), 2.04 (s, 3H).

ESI-MS m/z: Calcd. for C₄₁H₄₄N₄O₁₀S: 784.8 Found (M+H⁺): 785.3.

35: ¹H-NMR (300 MHz, CDCl₃): 8 d 6.78 (s, 1H), 6.46 (s, 1H), 6.40 (s, 1H), 6.02 (d, 2H), 5.02 (d, 1H), 4.47 (bp, 1H), 4.34 (s, 1H), 4.23 (d, 1H), 4.20 (d, 1H), 4.13-4.11 (m, 1H), 3.91 (s, 3H), 3.82 (s, 3H), 3.76 (s, 3H), 3.60 (s, 3H), 3.51 (d, 1H), 3.45-3.42 (m, 1H), 3.17-3.09 (m, 1H), 2.96-2.93 (m, 2H), 2.85-2.81 (m, 1H), 2.71-2.61 (m, 1H), 2.53-2.48 (m, 1H), 2.34-2.01 (m, 2H), 2.28 (s, 3H), 2.24 (s, 3H), 2.20 (s, 3H), 2.04 (s, 3H).

ESI-MS m/z: Calcd. for C₄₂H₄₆N₄O₁₀S: 798.3 Found (M+H⁺): 799.2

36: ¹H-NMR (300 MHz, CDCl₃): δ 6.76 (s, 1H), 6.47(s, 1H), 6.42 (s, 1H), 6.01 (d, 2H), 5.41 (bs, 1H), 5.01 (d, 1H), 4.47 (bp, 1H), 4.33 (s, 1H), 4.22 (d, 1H), 4.20 (d, 1H), 4.12 (dd, 1H), 3.90 (s, 3H), 3.82 (s, 3H), 3.61 (s, 3H), 3.50 (d, 1H), 3.44-3.42 (m, 1H), 3.14-3.06 (m, 1H), 3.00-2.87 (m, 2H), 2.82-2.78 (m, 1H), 2.67-2.56 (m, 1H), 2.50-2.44 (m, 1H), 2.32-2.11 (m, 2H), 2.28 (s, 3H), 2.23 (s, 3H), 2.20 (s, 3H), 2.04 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.6, 168.1, 164.3, 151.7, 148.6, 145.3, 144.5, 144.2, 141.2, 140.1, 131.4, 130.2, 129.0, 127.6, 125.6, 124.3, 121.3, 118.1, 114.1, 109.7, 101.8, 64.7, 61.2, 60.0, 59.7, 59.4, 59.1, 55.1, 54.9, 54.5, 42.2, 41.9, 41.7, 39.5, 28.7, 24.1, 20.2, 15.8, 9.7.

ESI-MS m/z: Calcd. for C₄₁H₄₄N₄O₁₀S: 784.8 Found (M+H⁺): 785.3.

EXAMPLE 28

37. (Method E) ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 1H); 6.47 (s, 1H); 6.40 (s, 1H); 6.01 (dd, 2H); 5.76 (s, 1H); 5.02 (d, 1H); 4.55 (s, 1H); 4.32 (s, 1H); 4.27 (d, 1H); 4.19 (d, 1H); 4.12 (dd, 1H); 3.98 (q, 2H); 3.78 (s, 3H); 3.59 (s, 3H); 3.51 (d, 1H); 3.42 (s, 1H); 3.15-3.06 (m, 1H); 2.94-2.92 (m, 2H); 2.81-2.75 (m, 1H); 2.68-2.58 (m, 1H); 2.56-2.42 (m, 1H); 2.39-2.10 (m, 2H); 2.32 (s, 3H); 2.26 (s, 3H); 2.19 (s, 3H); 2.03 (s, 3H); 1.37 (t, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.8, 167.9, 148.0, 147.5, 146.3, 143.2, 141.7, 141.6, 141.5, 132.7, 131.0, 130.1, 129.5, 129.0, 128.6, 121.3, 120.9, 118.3, 114.2, 112.8, 111.3, 102.1, 68.3, 64.3, 61.3, 60.5, 60.2, 59.8, 55.4, 54.9, 54.8, 39.9, 29.6, 29.1, 24.4, 22.8, 20.6, 16.0, 14.3, 9.6.

ESI-MS m/z: Calcd. for C₄₂H₄₆N₄O₁₀S: 798.2 Found (M+H⁺): 799.3.

38. (Method E): ¹H-NMR (300 MHz, CDCl₃): δ 6.72 (s, 1H); 6.47 (s, 1H); 6.40 (s, 1H); 6.02 (dd, 2H); 5.02 (d, 1H); 4.50 (s, 1H); 4.32 (s, 1H); 4.24 (d, 1H); 4.20 (d, 1H); 4.13 (dd, 1H); 3.99 (q, 2H); 3.96 (q, 2H); 3.83 (s, 3H); 3.60 (s, 3H); 3.51 (d, 1H); 3.42 (s, 1H); 3.15-3.06 (m, 1H); 2.96-2.93 (m, 2H); 2.84-2.78 (m, 1H); 2.70-2.58 (m, 1H); 2.53-2.42 (m, 1H); 2.33-2.11 (m, 2H); 2.28 (s, 3H); 2.25 (s, 3H); 2.20 (s, 3H); 2.04 (s, 3H); 1.40 (t, 3H); 1.37 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.8, 168.2, 151.0, 147.5, 147.0, 145.5, 141.4, 140.4, 131.4, 130.4, 129.0, 128.5, 128.4, 124.4, 121.5, 118.3, 114.2, 112.8, 111.0, 102.0, 68.3, 64.3, 61.5, 60.0, 59.4, 55.4, 55.3, 54.9, 54.5, 42.2, 42.1, 41.9, 39.8, 29.5, 29.2, 24.4, 22.8, 20.4, 16.4, 16.0, 14.3, 9.8.

ESI-MS m/z: Calcd. for C₄₄H₅₀N₄O₁₀S: 826.3 Found (M+H⁺): 827.3.

EXAMPLE 29

39. (Method E) ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 1H); 6.48 (s, 1H); 6.40 (s, 1H); 6.01 (dd, 2H); 5.74 (s, 1H); 5.02 (d, 1H); 4.55 (s, 1H); 4.31 (s, 1H); 4.27 (d, 1H); 4.18 (d, 1H); 4.11 (dd, 1H); 3.84 (q, 2H); 3.78 (s, 3H); 3.59 (s, 3H); 3.51 (d, 1H); 3.41 (s, 1H); 3.16-3.06 (m, 1H); 2.96-2.92 (m, 2H); 2.81-2.73 (m, 1H); 2.68-2.58 (m, 1H); 2.54-2.42 (m, 1H); 2.39-2.10 (m, 2H); 2.31 (s, 3H); 2.25 (s, 3H); 2.19 (s, 3H); 2.03 (s, 3H); 1.80-1-71 (m, 2H); 0.96 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.8, 167.9, 148.0, 147.5, 146.3, 143.2, 141.7, 141.6, 141.5, 131.0, 130.1, 129.5, 129.0, 128.6, 121.3, 120.9, 118.3, 114.2, 112.8, 111.3, 102.1, 70.5, 61.3, 60.5, 60.2, 60.0, 59.8, 59.7, 55.5, 54.9, 54.8, 42.3, 42.1, 41.8, 39.9, 29.9, 24.4, 22.5, 20.6, 16.0, 10.5, 9.9.

ESI-MS m/z: Calcd. for C₄₃H₄₈N₄O₁₀S: 812.3 Found (M+H⁺): 813.3.

40. (Method E). ¹H-NMR (300 MHz, CDCl₃): δ 6.77 (s, 1H); 6.47 (s, 1H); 6.40 (s, 1H); 6.03 (dd, 2H); 5.02 (d, 1H); 4.52 (s, 1H); 4.32 (s, 1H); 4.22 (d, 1H); 4.19 (d, 1H); 4.12 (dd, 1H); 3.87-3.80 (m, 4H); 3.82 (s, 3H); 3.59 (s, 3H); 3.51 (d, 1H); 3.43 (s, 1H); 3.15-3.06 (m, 1H); 2.96-2.93 (m, 2H); 2.84-2.74 (m, 1H); 2.68-2.58 (m, 1H); 2.53-2.42 (m, 1H); 2.38-2.07 (m, 2H); 2.28 (s, 3H); 2.24 (s, 3H); 2.20 (s, 3H); 2.04 (s, 3H); 1.83-1.72 (m, 4H); 1.10 (t, 3H); 0.96 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.8, 168.2, 151.2, 147.8, 147.1, 145.5, 141.7, 141.4, 131.4, 130.4, 128.6, 127.8, 125.4, 124.4, 121.5, 118.3, 114.2, 113.0, 111.3, 102.0, 74.3, 70.5, 61.4, 60.0, 59.6, 59.5, 55.5, 55.4, 54.9, 42.2, 42.1, 41.9, 39.8, 31.7, 29.9, 24.4, 24.2, 22.8, 22.5, 20.4, 16.0, 14.3, 11.1, 10.5, 9.8.

ESI-MS m/z: Calcd. for C₄₆H₅₄N₄O₁₀S: 854.3 Found (M+H⁺): 855.3.

EXAMPLE 30

Compounds 41 and 42 were obtained using Method E.

41: ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 1H); 6.48 (s, 1H); 6.40 (s, 1H); 6.04-5.92 (m, 1H); 6.01 (dd, 2H); 5.72 (s, 1H); 5.31 (dd, 1H); 5.22 (dd, 1H); 5.02 (d, 1H); 4.55 (s, 1H); 4.49 (d, 2H); 4.32 (s, 1H); 4.27 (d, 1H); 4.18 (d, 1H); 4.12 (dd, 1H); 3.78 (s, 3H); 3.60 (s, 3H); 3.51 (d, 1H); 3.41 (s, 1H); 3.16-3.06 (m, 1H); 2.95-2.92 (m, 2H); 2.82-2.74 (m, 1H); 2.67-2.58 (m, 1H); 2.52-2.42 (m, 1H); 2.37-2.10 (m, 2H); 2.32 (s, 3H); 2.26 (s, 3H); 2.19 (s, 3H); 2.03 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.8, 167.9, 148.0, 147.2, 143.2, 141.5, 140.3, 133.4, 131.0, 129.5, 128.6, 126.8, 121.3, 120.9, 118.4, 118.3, 117.9, 114.2, 113.4, 111.2, 102.1, 69.9, 64.7, 61.3, 60.5, 60.2, 59.8, 59.7, 55.5, 54.9, 54.8, 42.4, 42.0, 41.9, 41.8, 39.9, 29.9, 29.2. 24.4, 20.6, 16.0, 9.9.

ESI-MS m/z: Calcd. for C₄₃H₄₆N₄O₁₀S: 810.2 Found (M+H⁺): 811.2.

42: ¹H-NMR (300 MHz, CDCl₃): δ 6.79 (s, 1H); 6.48 (s, 1H); 6.40 (s, 1H); 6.16-5.92 (m, 2H); 6.03 (dd, 2H); 5.45 (dd, 1H); 5.31 (dd, 1H); 5.24 (dd, 1H); 5.21 (dd, 1H); 5.02 (d, 1H); 4.82-4.77 (m, 1H); 4.53 (s, 1H); 4.49 (d, 2H); 4.37-4.31 (m, 1H); 4.32 (s, 1H); 4.24 (d, 1H); 4.17 (d, 1H); 4.12 (dd, 1H); 3.82 (s, 3H); 3.60 (s, 3H); 3.51 (d, 1H); 3.42 (s, 1H); 3.15-3.06 (m, 1H); 2.96-2.93 (m, 2H); 2.84-2.74 (m, 1H); 2.68-2.58 (m, 1H); 2.53-2.42 (m, 1H); 2.34-2.11 (m, 2H); 2.28 (s, 3H); 2.23 (s, 3H); 2.19 (s, 3H); 2.03 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.8, 169.5, 150.7, 149.0, 147.2, 146.3, 141.5, 140.3, 134.8, 133.4, 131.4, 130.5, 128.5, 124.9, 124.7, 121.4, 118.2, 118.0, 116.9, 114.2, 113.4, 111.2, 102.1, 73.1, 69.8, 61.4, 60.0, 59.6, 59.5, 55.4, 55.3, 54.8, 42.3, 42.1, 41.9, 39.8, 29.9, 29.1, 24.4, 20.5, 16.0, 9.8.

ESI-MS m/z: Calcd. for C₄₆H₅₀N₄O₁₀S: 850.3 Found (M+H⁺): 851.3.

EXAMPLE 31

Compounds 43 and 44 were obtained using Method E

43: ¹H-NMR (300 MHz, CDCl₃): δ 7.38-7.26 (m, 5H); 6.59 (s, 1H); 6.51 (s, 1H); 6.41 (s, 1H); 6.02 (dd, 2H); 5.73 (s, 1H); 5.03 (s, 2H); 5.01 (d, 1H); 4.56 (s, 1H); 4.32 (s, 1H); 4.27 (d, 1H); 4.18 (d, 1H); 4.12 (dd, 1H); 3.78 (s, 3H); 3.61 (s, 3H); 3.51 (d, 1H); 3.42 (s, 1H); 3.13-3.06 (m, 1H); 2.94-2.92 (m, 2H); 2.80-2.72 (m, 1H); 2.62-2.53 (m, 1H); 2.47-2.37 (m, 1H); 2.34-2.10 (m, 2H); 2.32 (s, 3H); 2.26 (s, 3H); 2.19 (s, 3H); 2.03 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.8, 169.5, 168.3, 148.0, 147.3, 145.5, 143.2, 141.5, 140.3, 137.3, 132.4, 131.0, 128.6, 127.9, 127.3, 127.0, 121.3, 120.9, 118.3, 114.2, 113.9, 111.4, 102.1, 70.9, 64.7, 61.3, 60.5, 60.2, 59.8, 59.7, 55.5, 54.9, 54.8, 42.3, 42.0, 41.8, 39.9, 29.9, 29.1, 24.4, 20.6, 16.0, 9.9.

ESI-MS m/z: Calcd. for C₄₇H₄₈N₄O₁₀S: 860.3 Found (M+H⁺): 861.3.

44: ¹H-NMR (300 MHz, CDCl₃): δ 7.47-7.25 (m, 10H); 6.81 (s, 1H); 6.48 (s, 1H); 6.41 (s, 1H); 6.01 (dd, 2H); 5.32 (d, 1H); 5.03 (s, 2H); 5.01 (d, 1H); 4.84 (d, 1H); 4.50 (s, 1H); 4.32 (s, 1H); 4.21 (d, 1H); 4.19 (d, 1H); 4.13 (dd, 1H); 3.86 (s, 3H); 3.60 (s, 3H); 3.49 (d, 1H); 3.40 (s, 1H); 3.15-3.06 (m, 1H); 2.96-2.93 (m, 2H); 2.81-2.71 (m, 1H); 2.64-2.51 (m, 1H); 2.50-2.40 (m, 1H); 2.33-2.11 (m, 2H); 2.32 (s, 3H); 2.04 (s, 3H); 2.02 (s, 3H); 2.00 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.7, 168.3, 149.2, 147.4, 147.3, 145.5, 141.4, 140.3, 138.1, 137.2, 131.5, 130.3, 128.8, 128.7, 128.6, 128.2, 128.1, 127.9, 127.3, 127.0, 125.0, 124.9, 121.4, 118.2, 114.2, 114.0, 111.3, 102.0, 74.3, 70.9, 64.9, 61.4, 60.1, 60.0, 59.7, 59.5, 55.5, 55.4, 54.8, 42.2, 42.1, 41.7, 39.7, 31.7, 29.9, 24.4, 22.8, 20.1, 16.0, 14.3, 9.8.

ESI-MS m/z: Calcd. for C₅₄H₅₄N₄O₁₀S: 950.3 Found (M+H⁺): 951.3.

EXAMPLE 32

The reaction was performed with 1.0 equiv. of MeI and 1.0 equiv. of CS₂CO₃ (Method E). After chromatographic purification starting material (16%) was recuperated.

45. ¹H-NMR (300 MHz, CDCl₃): d 6.76 (s, 1H), 6.47(s, 1H), 6.42 (s, 1H), 6.01 (d, 2H), 5.41 (bs, 1H), 5.01 (d, 1H), 4.47 (bp, 1H), 4.33 (s, 1H), 4.22 (d, 1H), 4.20 (d, 1H), 4.12 (dd, 1H), 3.90 (s, 3H), 3.82 (s, 3H), 3.61 (s, 3H), 3.50 (d, 1H), 3.44-3.42 (m, 1H), 3.14-3.06 (m, 1H), 3.00-2.87 (m, 2H), 2.82-2.78 (m, 1H), 2.67-2.56 (m, 1H), 2.50-2.44 (m, 1H), 2.32-2.11 (m, 2H), 2.28 (s, 3H), 2.23 (s, 3H), 2.20 (s, 3H), 2.04 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): 172.6, 168.1, 164.3, 151.7, 148.6, 145.3, 144.5, 144.2, 141.2, 140.1, 131.4, 130.2, 129.0, 127.6, 125.6, 124.3, 121.3, 118.1, 114.1, 109.7, 101.8, 64.7, 61.2, 60.0, 59.7, 59.4, 59.1, 55.1, 54.9, 54.5, 42.2, 41.9, 41.7, 39.5, 28.7, 24.1, 20.2, 15.8, 9.7.

ESI-MS m/z: Calcd. for C₄₆H₅₂N₄O₁₂S: 884.3 Found (M+H⁺): 985.3.

EXAMPLE 33

Compound 46 was obtained with 15 equiv. of isopropyl bromide and 15 equiv, of CS₂CO₃ (Method E)

46. ¹-H-NMR (300 MHz, CDCl₃): d 6.75 (s, 1H), 6.68 (s, 1H), 6.57 (s, 1H), 6.03 (d, 1H), 5.96(d, 1H); 4.99 (d, 1H), 4.86-4.80 (m, 1H); 4.51 (s, 1H), 4.35-4.31 (m, 2H), 4.18 (s, 1H), 4.11 (d, 1H), 3.80 (s, 3H), 3.58 (s, 3H), 3.48 (d, 1H), 3.41 (s, 1H), 3.15-3.08 (m, 1H), 2.95-2.93 (m, 2H), 2.82-2.74 (m, 1H), 2.68-2.48 (m, 2H); 2.27 (s, 3H), 2.26 (s, 3H), 2.23 (s, 3H), 2.17-2.12 (m, 1H); 2.04 (s, 3H); 1.50 (s, 9H); 1.45 (d, 3H); 1.14 (d, 3H).

ESI-MS m/z: Calcd. for C₄₈H₅₆N₄O₁₂S: 912.3 Found (M+H⁺): 913.3.

EXAMPLE 34

Method F: To a solution of 1 equiv. of starting material in CH₂Cl₂/H₂O/TFA 2:1:3.3 (0.013M) was stirred at room temperature for 15 min. The reaction was followed by TLC and neutralised with NaHCO₃, extracted with CH₂Cl₂ and the organic layers dried with Na₂SO₄. Flash chromatography gives pure compounds.

47. was obtained using Method F ¹H-NMR (300 MHz, CDCl₃): δ 6.93 (s, 1H); 6.48 (s, 1H); 6.42 (s, 1H); 6.02 (dd, 2H); 5.39 (s, 1H); 5.02 (d, 1H); 4.47 (s, 1H); 4.33 (s, 1H); 4.18 (d, 1H); 4.13 (dd, 1H); 3.93 (d, 1H); 3.79 (s, 3H); 3.62 (s, 3H); 3.52 (d, 1H); 3.46-3.44 (m, 1H); 3.12-3.04 (m, 1H); 2.98 (d, 2H); 2.83-2.76 (m, 1H); 2.64-2.57 (m, 1H); 2.51-2.46 (m, 1H); 2.24-2.03 (m, 2H); 2.32 (s, 3H); 2.31 (s, 3H); 2.17 (s, 3H); 2.06 (s, 3H); 1.56 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 168.4, 151.3, 148.3, 145.6, 144.8, 144.5, 141.5, 140.4, 131.6, 130.5, 129.4, 127.1, 125.7, 124.5, 121.4, 118.1, 114.3, 114.2, 113.6, 109.9, 102.0, 83.4, 67.4, 61.4, 60.2, 60.0, 59.8, 59.3, 55.9, 55.8, 54.7, 42.4, 42.1, 41.8, 39.8, 29.9, 29.0, 27.8, 24.2, 20.3, 16.0, 9.8.

ESI-MS m/z: Calcd. for C₄₅H₅₀N₄O₁₂S: 870.3 Found (M+H⁺): 871.3.

EXAMPLE 35

48 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): d 6.76 (s, 1H), 6.46 (s, 1H), 6.44 (s, 1H), 6.04 (d, 1H), 5.97 (d, 1H); 5.42 (s, 1H); 5.01 (d, 1H), 4.89-4.80 (m, 1H); 4.53 (s, 1H), 4.34 (dd, 1H); 4.31 (s, 1H), 4.19 (d, 1H), 4.12 (dd, 1H), 3.80 (s, 3H), 3.61 (s, 3H), 3.49 (d, 1H), 3.42 (s, 1H), 3.12-3.04 (m, 1H), 2.95 (d, 2H), 2.78-2.73 (m, 1H), 2.64-2.47 (m, 2H); 2.30-2.10 (m, 2H); 2.28 (s, 3H), 2.25 (s, 3H), 2.23 (s, 3H), 2.04 (s, 3H); 1.45 (d, 3H); 1.14 (d, 3H).

ESI-MS m/z: Calcd. for C₄₃H₄₈N₄O₁₀S: 812.3 Found (M+H⁺): 813.3.

EXAMPLE 36

After chromatographic purification, starting material (33%) was recuperated. Compound 36 has been previously described.

Other chemical transformations:

EXAMPLE 37

Compound 47 was acylated following method B.

49. ¹H-NMR (300 MHz, CDCl₃): δ 7.80 (d, 1H); 7.56-7.54 (m, 2H); 7.41-7.39 (m, 3H); 6.93 (s, 1H); 6.69 (s, 1H); 6.60 (d, 1H); 6.57 (s, 1H); 6.00 (dd, 2H); 5.02 (d, 1H); 4.45 (s, 1H); 4.34 (s, 1H); 4.18 (d, 1H); 4.13 (dd, 1H); 3.93 (d, 1H); 3.80 (s, 3H); 3.56 (s, 3H); 3.52 (d, 1H); 3.46-3.43 (m, 1H); 3.15-3.06 (m, 1H); 2.98-2.96 (m, 2H); 2.86-2.80 (m, 1H); 2.64-2.59 (m, 1H); 2.54-2.46 (m, 1H); 2.35-2.05 (m, 2H); 2.33 (s, 3H); 2.31 (s, 3H); 2.18 (s, 3H); 2.05 (s, 3H); 1.53 (s, 9H).

ESI-MS m/z: Calcd. for C₅₄H₅₆N₄O₁₃S: 1000.3 Found (M+H⁺): 1001.3.

EXAMPLE 38

To a solution of compound 42 in THF/MeOH 1:1 were added 2 equiv of KOH. The reaction mixture was stirred at room temperature for 5 h. After this time the reaction was quenched with NaCl or diluted aqueous solution of HCl, extracted with CH₂Cl₂. The organic layer was dried with Na₂SO₄. Chromatography gives pure compound 50 (79%).

50. ¹H-NMR (300 MHz, CDCl₃): δ 6.81 (s, 1H), 6.47 (s, 1H), 6.43 (s, 1H), 6.17-5.90 (m, 2H), 5.94 (d, 2H), 5.45-5.22 (m, 4H), 4.98 (d, 1H), 4.83-4.77 (m, 1H), 4.56-4.27 (m, 5H), 4.16-4.02 (m, 3H), 3.84 (s, 3H), 3.58 (bs, 4H), 3.44-3.40 (m, 1H), 3.20-2.16 (m, 8H), 2.31 (s, 3H), 2.25 (s, 3H), 2.19 (s, 3H).

ESI-MS m/z: Calcd. for C₄₄H₄₈N₄O₉S: 808.3 Found (M+H⁺): 809.2.

EXAMPLE 39

To a solution of compound 6 in MeOH/THF 3:4 (0.011M) at room temperature were added 150 equiv. of Et₃N. After 7 days the solvent was evaporated. Flash chromatography gives pure compound 51.

51. ¹H-NMR (300 MHz, CDCl₃): δ 6.95 (s, 1H), 6.49 (s, 1H), 6.40 (bs, 1H), 6.02 (dd, 2H), 5.42 (bs, 1H), 5.02 (d, 1H), 4.45 (bs, 1H), 4.35 (s, 1H), 4.21-4.10 (m, 2H), 3.84-3.68 (m, 4H), 3.62 (s, 3H), 3.53 (bd, 1H), 3.48-3.44 (m, 1H), 3.16-2.75 (m, 4H), 2.67-2.14 (m, 4H), 2.38 (s, 3H), 2.35 (s, 3H), 2.31 (s, 3H), 2.16 (s, 3H), 2.01 (s, 3H).

ESI-MS m/z: Calcd. for C₄₂H₄₄N₄O₁₁S: 812.3 Found (M+H⁺): 813.3.

EXAMPLE 40

To a solution of Et-770 (1) (1.0 equiv.) in MeOH (0.032M) at room temperature under Argon, were added RuCl₂(PPh₃)₃ (0.1 equiv.) and H₂O₂ (8 equiv.). The reaction mixture was stirred at room temperature for 4 h. After this time, it was diluted with CH₂Cl₂, washed with brine and the organic layer was dried over Na₂SO₄. Flash chromatography gives compound 52.

52. ¹H-NMR (300 MHz, CDCl₃): δ 6.48(s, 1H); 6.43(s, 1H); 6.05(s, 1H); 5.99(s, 1H); 5.42(s, 1H); 4.92(d, 1H); 4.50(s, 1H); 4.22(s, 1H); 4.18-4.15(m, 1H); 4.12-3.98(m, 2H); 4.10(s, 3H); 3.61(s, 3H); 3.58-3.55(m, 1H); 3.42-3.37(m, 2H); 3.12-3.03(m, 1H); 2.90-2.59(m, 3H); 2.55-2.27(m, 4H); 2.24(s, 3H); 2.21(s, 3H); 2.04(s, 3H); 2.02(s, 3H).

ESI-MS m/z: Calcd. for C₄₀H₄₀N₄O₁₁S: 784.2. Found (M+Na⁺): 807.2.

EXAMPLE 41

A suspension of 1, coevaporated twice with anhydrous toluene, in CH₃CN (0.03M) under Argon was cooled at −10° C. At this temperature were added 5 equiv. of CCl₄, 2.1 equiv. of ^(i)Pr₂NEt, 0.1 equiv. of DMAP and 1.45 equiv of dibenzyl phosphite. After 1 h the reaction was quenched with 1.2 equiv. of KH₂PO₄ (0.5M). The reaction mixture was warmed up to room temperature, stirred for 5 min, diluted with EtOAc and washed with water. The organic layers were dried with Na₂SO₄. Flash chromatography gives pure compound 53 (75%).

53. ¹H-NMR (300 MHz, CDCl₃): δ 7.29 (s, 10H), 6.71 (s, 1H), 6.59 (s, 1H), 6.52 (s, 1H), 6.00 (d, 2H), 5.76 (s, 1H), 5.12-5.07 (m, 2H), 5.02 (d, 1H), 4.57 (bs, 1H), 4.32 (s, 1H), 4.27 (d, 1H), 4.18 (d, 1H), 4.11 (bd, 1H), 3.78 (s, 3H), 3.50 (bs, 4H), 3.44-3.39 (m, 1H), 3.12-3.03 (m, 1H), 2.95-2.92 (m, 2H), 2.81-2.72 (m, 1H), 2.60-2.04 (m, 4H), 2.32 (s, 3H), 2.27 (s, 3H), 2.20 (s, 3H), 2.04 (s, 3H).

ESI-MS m/z: Calcd. for C₅₄H₅₅N₄O₁₃PS: 1030.3 Found (M+H⁺): 1031.3.

EXAMPLE 42

Method G: To a solution of Et-770 (1) in CH₃CN (0.016M) at room temperature under Argon, were added 200 equiv. of the aldehyde (37 wt. % in water) and 10 equiv. of NaCNBH₃. After 1 h 10 min 40 equiv. of acetic acid were added. The reaction mixture was stirred for 2 h more. After this time, it was diluted with CH₂Cl₂, neutralised with NaHCO₃ and extracted with CH₂Cl₂. The organic layers were dried over Na₂SO₄. Flash chromatography gives pure compounds.

54 was obtained following method G. ¹H-NMR (300 MHz, CDCl₃): δ 6.47 (s, 1H), 6.45 (s, 1H), 6.17 (s, 1H), 6.02 (dd, 2H), 5.73 (bs, 1H), 5.44 (bs, 1H), 4.94 (d, 1H), 4.60 (bs, 1H), 4.35 (d, 1H), 4.26 (d, 1H), 4.07 (d 1H), 3.88-3.82 (m, 1H), 3.79 (s, 3H), 3.56 (s, 3H), 3.52 (bd, 1H), 3.42-3.39 (m, 1H), 3.20 (bp, 1H), 3.00-2.44 (m, 5H), 2.35-2.16 (m, 2H), 2.31 (s, 3H), 2.24 (s, 3H), 2.21 (bs, 3H), 2.16 (s, 3H), 2.02 (s, 3H).

ESI-MS m/z: Calcd. for C₄₁H₄₄N₄O₁₀S: 784.3. Found (M+H⁺): 785.2.

EXAMPLE 43

55 was obtained following method G ¹H-NMR (300 MHz, CD₃OD): δ 6.41 (s, 1H), 6.35 (s, 1H), 6.21 (s, 1H), 6.09 (d, 2H), 4.97 (d, 1H), 4.67 (bs, 1H), 4.36 (bs, 2H), 4.27 (d, 1H), 3.95 (dd 1H), 3.73 (s, 3H), 3.53 (s, 3H), 3.45-3.41 (m, 2H), 2.98-2.47 (m, 6H), 2.37-2.03 (m, 4H), 2.33 (s, 3H), 2.25 (s, 3H), 2.07 (s, 3H), 2.03 (s, 3H), 0.88 (t, 3H).

ESI-MS m/z: Calcd. for C₄₂H₄₆N₄O₁₀S: 798.3. Found (M+H⁺): 799.2.

EXAMPLE 44

56 was obtained following method G. ¹H-NMR (300 MHz, CDCl₃): δ 6.46 (s, 1H), 6.43 (s, 1H), 6.23 (s, 1H), 6.03 (d, 2H), 5.86 (s, 1H), 5.43 (s, 1H), 4.96 (d, 1H), 4.63 (bs, 1H), 4.46 (d, 1H), 4.27 (d, 1H), 4.08 (d 1H), 3.95-3.85 (m, 1H), 3.84 (s, 3H), 3.56 (d, 1H), 3.52 (s, 3H), 3.46-3.41 (m, 1H), 3.00-2.85 (m, 3H), 2.72-2.64 (m, 2H), 2.50-2.42 (m, 1H), 2.36-2.03 (m, 4H), 2.33 (s, 6H), 2.07 (s, 3H), 2.03 (s, 3H), 1.35-1.24 (m, 2H), 0.87 (t, 3H).

ESI-MS m/z: Calcd. for C₄₃H₄₈N₄O₁₀S: 812.3. Found (M+H⁺): 813.3.

EXAMPLE 45

Method H: To a solution of 1 equiv. of starting material in CH₃CN/H₂O 3:2 (0.009M) were added 30 equiv. of AgNO₃. After 24 h the reaction was quenched with a mixture 1:1 of saturated solutions of brine and NaHCO₃, stirred for 10 min and diluted and extracted with CH₂Cl₂. The organic layer was dried over Na₂SO₄. Chromatography gives pure compounds.

57 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 6.60 (s, 2H); 6.57 (s, 1H); 5.97 (dd, 2H); 5.70 (s, 1H); 5.12 (d, 1H); 4.82 (s, 1H); 4.48 (d, 1H); 4.47 (s, 1H); 4.16 (d, 1H); 4.04 (dd, 1H); 3.79 (s, 3H); 3.58 (d, 1H); 3.54 (s, 3H); 3.23-3.20 (m, 1H); 3.18-3.09 (m, 1H); 2.88-2.86 (m, 2H); 2.86-2.78 (m, 1H); 2.66-2.58 (m, 1H); 2.52-2.44 (m, 1H); 2.35-2.12 (m, 2H); 2.32 (s, 3H); 2.27 (s, 3H); 2.23 (s, 3H); 2.17 (s, 3H); 2.01 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 168.9, 148.3, 147.6, 145.1, 141.2, 140.4, 139.1, 138.4, 131.4, 130.8, 128.7, 128.6, 122.9, 122.3, 121.6, 120.9, 120.6, 115.8, 111.7, 101.6, 82.0, 64.9, 61.4, 60.3, 57.8, 57.6, 55.9, 55.0, 54.9, 42.1, 41.3, 39.5, 29.6, 24.0, 20.5, 15.7, 9.6.

ESI-MS m/z: Calcd. for C₄₁H₄₅N₃O₁₂S: 803.2 Found (M−H₂O+H⁺): 786.2.

EXAMPLE 46

58 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.60 (s, 1H); 6.59 (s, 1H); 6.57 (s, 1H); 5.97 (dd, 2H); 5.72 (s, 1H); 5.12 (d, 1H); 4.81 (s, 1H); 4.47 (d, 1H); 4.47-4.45 (m, 1H); 4.16 (d, 1H); 4.03 (dd, 1H); 3.79 (s, 3H); 3.58 (d, 1H); 3.53 (s, 3H); 3.26-3.20 (m, 1H); 3.18-3.09 (m, 1H); 2.88-2.86 (m, 2H); 2.86-2.78 (m, 1H); 2.69-2.58 (m, 1H); 2.52-2.44 (m, 1H); 2.48 (t, 2H); 2.35-2.12 (m, 2H); 2.32 (s, 3H); 2.27 (s, 3H); 2.17 (s, 3H); 2.01 (s, 3H); 1.78-1.67 (m, 2H); 1.00 (t, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 171.8, 167.2, 148.6, 147.9, 145.4, 141.5, 141.5, 140.7, 138.7, 132.9, 132.4, 131.7, 131.0, 130.5, 128.8, 127.8, 122.6, 121.1, 120.8, 116.2, 112.0, 101.9, 82.3, 65.1, 61.6, 60.5, 58.0, 56.1, 55.3, 55.1, 42.5, 41.6, 39.8, 29.9, 28.9, 24.3, 22.8, 20.6, 18.7, 16.0, 14.3, 13.7, 9.8.

ESI-MS m/z: Calcd. for C₄₃H₄₉N₃O₁₂S: 814.3 Found (M⁺−H₂O): 796.3.

EXAMPLE 47

59 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 1H); 6.58 (s, 1H); 6.55 (s, 1H); 5.96 (dd, 2H); 5.69 (s, 1H); 5.11 (d, 1H); 4.80 (s, 1H); 4.47-4.45 (m, 2H); 4.14 (d, 1H); 4.02 (dd, 1H); 3.78 (s, 3H); 3.56 (d, 1H); 3.53 (s, 3H); 3.24-3.18 (m, 1H); 3.14-3.04 (m, 1H); 2.86-2.84 (m, 2H); 2.86-2.78 (m, 1H); 2.69-2.58 (m, 1H); 2.52-2.44 (m, 1H); 2.48 (t, 2H); 2.35-2.12 (m, 2H); 2.31 (s, 3H); 2.26 (s, 3H); 2.16 (s, 3H); 2.01 (s, 3H); 1.73-1.61 (m, 2H); 1.40-1.14 (m, 11H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 171.8, 148.4, 147.7, 145.1, 142.9, 141.3, 140.5, 138.5, 132.7, 131.5, 129.9, 128.6, 122.4, 121.7, 120.9, 115.8, 111.7, 101.6, 82.1, 64.9, 61.4, 60.3, 57.8, 57.7, 55.9, 55.1, 54.9, 42.2, 41.4, 39.6, 33.9, 31.6, 29.6, 28.9, 28.6, 21.0, 24.0, 22.5, 20.4, 15.7, 14.0, 9.6.

ESI-MS m/z: Calcd. for C₄₇H₅₇N₃O₁₂S: 888.0 Found (M⁺−H₂O): 870.3.

EXAMPLE 48

60 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.60 (s, 1H); 6.58 (s, 1H); 6.56 (s, 1H); 5.96 (dd, 2H); 5.72 (s, 1H); 5.12 (d, 1H); 4.81 (s, 1H); 4.48 (d, 1H); 4.47-4.45 (m, 1H); 4.16 (d, 1H); 4.03 (dd, 1H); 3.79 (s, 3H); 3.58 (d, 1H); 3.53 (s, 3H); 3.24-3.19 (m, 1H); 3.14-3.09 (m, 1H); 2.87-2.84 (m, 2H); 2.86-2.78 (m, 1H); 2.69-2.58 (m, 1H); 2.52-2.44 (m, 1H); 2.49 (t, 2H); 2.37-2.12 (m, 2H); 2.31 (s, 3H); 2.27 (s, 3H); 2.17 (s, 3H); 2.01 (s, 3H); 1.73-1.62 (m, 2H); 1.40-1.20 (m, 27H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.2, 172.0, 168.5, 148.6, 147.9, 145.4, 143.2, 141.5, 140.7, 138.8, 132.8, 131.7, 129.4, 128.8, 125.3, 122.6, 121.9, 121.1, 116.0, 111.9, 101.9, 82.3, 65.1, 61.6, 60.5, 58.0, 57.8, 56.1, 55.3, 55.1, 53.6, 42.4, 41.5, 39.8, 34.2, 32.1, 31.7, 29.89, 29.85, 29.82, 29.7, 29.5, 29.4, 29.3, 29.2, 28.8, 25.3, 22.9, 22.8, 20.6, 16.0, 14.3, 9.8.

ESI-MS m/z: Calcd. for C₅₅H₇₃N₃O₁₂S: 1000.2 Found (M⁺−H₂O): 982.4.

EXAMPLE 49

61 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 7.80 (d, 1H); 7.57-7.54 (m, 2H); 7.40-7.38 (m, 3H); 6.68 (s, 1H); 6.60 (s, 2H); 6.59 (d, 1H); 5.96 (dd, 2H); 5.70 (s, 1H); 5.13 (d, 1H); 4.82 (s, 1H); 4.48 (d, 1H); 4.48-4.46 (m, 1H); 4.16 (d, 1H); 4.05 (dd, 1H); 3.79 (s, 3H); 3.59 (d, 1H); 3.55 (s, 3H); 3.25-3.20 (m, 1H); 3.18-3.09 (m, 1H); 2.88-2.85 (m, 2H); 2.86-2.78 (m, 1H); 2.70-2.60 (m, 1H); 2.56-2.44 (m, 1H); 2.35-2.08 (m, 2H); 2.32 (s, 3H); 2.28 (s, 3H); 2.17 (s, 3H); 2.01 (s, 3H).

ESI-MS m/z: Calcd. for C₄₈H₄₉N₃O₁₂S: 892.3 Found (M⁺−H₂O): 874.3.

EXAMPLE 50

62 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 7.75-7.73 (d, 2H), 7.66-7.61 (m, 2H), 7.40-7.33 (t, 2H), 7.30-7.27 (m, 2H), 6.63 (s, 1H), 6.57 (s, 1H), 6.54 (s, 1H), 5.96 (d, 2H), 5.98-5.85 (m, 1H), 5.58 (d, 1H), 5.30-5.18 (m, 2H), 5.10 (d, 1H), 4.87-4.02 (m, 9H), 3.80 (s, 3H), 3.64-3.57 (m, 1H), 3.44 (s, 3H), 3.16-2.42 (m, 11H), 2.34-2.17 (m, 2H), 2.34 (s, 3H), 2.27 (s, 3H), 2.17 (s, 3H), 2.04 (s, 3H).

ESI-MS m/z: Calcd. for C₆₀H₆₂N₄O₁₄S₂: 1126.4 Found (M−H₂O+H⁺): 1109.3.

EXAMPLE 51

63 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 2H), 6.56 (s, 1H), 5.96 (d, 2H), 5.96 (bs, 1H), 5.77 (s, 1H), 5.13 (s, 1H), 5.11 (d, 1H), 4.80 (bs, 1H), 4.47-4.43 (m, 3H), 4.28 (dd, 1H), 4.16 (d, 1H), 4.03 (dd, 1H), 3.78 (s, 3H), 3.57 (d, 1H), 3.53 (s, 3H), 3.22-3.10 (m, 3H), 2.92-2.46 (m, 9H), 2.36-2.17 (m, 2H), 2.31 (s, 3H), 2.26 (s, 3H), 2.17 (s, 3H), 2.01 (s, 3H), 1.76-1.65 (m, 3H), 1.50-148 (m, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 171.7, 168.5, 163.3, 148.2, 147.7, 145.1, 142.9, 141.2, 140.4, 138.3, 132.8, 131.5, 129.2, 128.6, 122.4, 121.6, 120.8, 118.0, 115.8, 111.6, 101.7, 82.0, 64.9, 61.9, 61.4, 60.3, 60.0, 57.7, 57.6, 55.9, 55.4, 55.1, 54.8, 42.2, 41.4, 40.5, 39.5, 33.5, 28.6, 28.1, 24.7, 24.0, 20.4, 15.8, 9.6.

ESI-MS m/z: Calcd. for C₄₉H₅₇N₅O₁₃S₂: 987.3 Found (M−H₂O+H⁺): 970.2.

EXAMPLE 52

64 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.70 (s, 1H), 6.60 (s, 1H), 6.59 (s, 1H), 6.04-5.89 (m, 1H), 5.97 (dd, 2H), 5.69 (s, 1H), 5.42-5.27 (m, 2H), 5.12 (d, 1H), 4.81 (s, 1H), 4.68 (d, 2H), 4.48-4.45 (m, 2H), 4.16 (d, 1H), 4.03 (dd, 1H), 3.79 (s, 3H), 3.57 (s, 3H), 3.59-3.57 (m, 1H), 3.21-3.10 (m, 2H), 2.93-2.79 (m, 3H), 2.68-2.60 (m, 1H), 2.52-2.47 (m, 1H), 2.32 (s, 3H), 2.38-2.17 (m, 2H), 2.27 (s, 3H), 2.17 (s, 3H), 2.02 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 168.4, 153.1, 148.3, 147.7, 145.1, 142.9, 141.3, 140.5, 138.7, 133.2, 131.5, 131.2, 129.1, 128.6, 122.0, 121.7, 120.9, 119.1, 117.9, 115.8, 111.9, 101.7, 82.1, 69.1, 64.9, 61.5, 60.3, 57.7, 57.7, 55.9, 55.2, 54.9, 42.2, 41.4, 39.5, 28.7, 24.0, 20.4, 15.8, 9.6.

ESI-MS m/z: Calcd. for C₄₃H₄₇N₃O₁₃S: 845.3 Found (M−H₂O+H⁺): 828.3.

EXAMPLE 53

65 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 7.40-7.33 (m, 5H); 6.69 (s, 1H); 6.60 (s, 1H); 6.57 (s, 1H); 5.96 (dd, 2H); 5.70 (s, 1H); 5.21 (s, 2H); 5.11 (d, 1H); 4.81 (s, 1H); 4.47 (d, 1H); 4.47-4.45 (m, 1H); 4.15 (d, 1H); 4.03 (dd, 1H); 3.79 (s, 3H); 3.58 (d, 1H); 3.54 (s, 3H); 3.23-3.20 (m, 1H); 3.18-3.09 (m, 1H); 2.87-2.85 (m, 2H); 2.86-2.78 (m, 1H); 2.69.2.58 (m, 1H); 2.52-2.44 (m, 1H); 2.36-2.12 (m, 2H); 2.31 (s, 3H); 2.27 (s, 3H); 2.17 (s, 3H); 2.01 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 168.9, 148.3, 147.6, 145.1, 141.2, 140.4, 139.1, 138.7, 131.4, 130.8, 128.7, 128.5, 122.1, 121.9, 121.1, 120.9, 120.6, 116.0, 112.1, 101.9, 82.3, 70.5, 65.1, 61.7, 60.5, 58.0, 57.9, 56.1, 55.3, 55.1, 42.4, 41.6, 39.7, 29.9, 29.5, 24.2, 22.9, 20.6, 16.0, 9.8.

ESI-MS m/z: Calcd. for C₄₇H₄₉N₃O₁₃S: 895.9 Found (M−H₂O+H⁺): 878.6.

EXAMPLE 54

66 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.68 (s, 1H); 6.60 (s, 1H); 6.57 (s, 1H); 5.97 (dd, 2H); 5.70 (s, 1H); 5.11 (d, 1H); 4.81 (s, 1H); 4.47 (d, 1H); 4.46 (s, 1H); 4.16 (d, 1H); 4.02 (dd, 1H); 3.79 (s, 3H); 3.58-3.56 (m, 1H); 3.57 (s, 3H); 3.23-3.20 (m, 1H); 3.18-3.09 (m, 1H); 2.87-2.84 (m, 2H); 2.86-2.78 (m, 1H); 2.66-2.58 (m, 1H); 2.52-2.44 (m, 1H); 2.36-2.12 (m, 2H); 2.32 (s, 3H); 2.27 (s, 3H); 2.17 (s, 3H); 2.02 (s, 3H); 1.50 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.2, 168.6, 151.8, 148.7, 147.9, 145.4, 143.1, 141.5, 140.7, 139.0, 133.0, 131.7, 129.4, 128.8, 122.3, 121.8, 121.1, 116.0, 112.1, 101.9, 83.6, 82.3, 65.1, 61.6, 60.5, 58.0, 57.8, 56.1, 55.4, 55.1, 42.4, 41.2, 39.8, 29.9, 28.9, 27.8, 24.2, 20.6, 16.0, 9.8.

ESI-MS m/z: Calcd. for C₄₄H₁₅N₃O₁₃S: 861.9 Found (M−H₂O+H⁺): 844.2.

EXAMPLE 55

67 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.61 (s, 1H), 6.47 (s, 1H), 6.40 (s, 1H), 5.98 (dd, 2H), 5.70 (s, 1H), 5.13 (d, 1H), 4.82 (s, 1H), 4.49-4.46 (m, 2H), 4.17 (bd, 1H), 4.05 (dd, 1H), 3.80 (s, 3H), 3.76 (s, 3H), 3.60 (s, 3H), 3.60-3.51 (m, 1H), 3.22-3.13 (m, 2H), 2.94-2.82 (m, 3H), 2.70-2.62 (m, 1H), 2.53-2.47 (m, 1H), 2.39-2.07 (m, 2H), 2.32 (s, 3H), 2.26 (s, 3H), 2.18 (s, 3H), 2.02 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.7, 148.0, 147.9, 146.7, 145.3, 143.1, 141.4, 140.7, 131.7, 129.3, 128.5, 126.6, 121.9, 121.1, 118.2, 116.0, 111.2, 110.6, 101.9, 82.3, 64.8, 61.5, 60.5, 58.0, 57.9, 56.1, 55.9, 55.1, 42.3, 41.6, 39.9, 29.2, 24.2, 20.6, 16.0, 9.8.

ESI-MS m/z: Calcd. for C₄₀H₄₅N₃O₁₁S: 775.8 Found (M−H₂O+H⁺): 758.2.

EXAMPLE 56

68 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.61 (s, 1H); 6.47 (s, 1H); 6.40 (s, 1H); 5.97 (dd, 2H); 5.69 (s, 1H); 5.12 (d, 1H); 4.82 (s, 1H); 4.48 (d, 1H); 4.47 (s, 1H); 4.16 (d, 1H); 4.04 (dd, 1H); 3.97 (q, 2H); 3.79 (s, 3H); 3.65 (d, 1H); 3.58 (s, 3H); 3.23-3.20 (m, 1H); 3.18-3.09 (m, 1H); 2.88-2.86 (m, 2H); 2.86-2.78 (m, 1H); 2.66-2.58 (m, 1H); 2.52-2.44 (m, 1H); 2.35-2.12 (m, 2H); 2.32 (s, 3H); 2.26 (s, 3H); 2.17 (s, 3H); 2.02 (s, 3H); 1.37 (t, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.2, 168.8, 165.4, 148.1, 145.8, 143.4, 141.2, 141.0, 135.0, 131.4, 130.1, 129.8, 129.0, 127.9, 121.0, 120.9, 120.7, 118.6, 115.4, 112.9, 102.0, 81.7, 61.9, 60.6, 58.0, 57.9, 57.7, 56.2, 55.2, 52.2, 42.4, 41.5, 32.9, 32.8, 23.8, 20.7, 19.4, 18.2, 16.6, 9.7.

ESI-MS m/z: Calcd. for C₄₁H₄₇N₃O₁₁S: 789.8 Found (M−H₂O+H⁺): 772.2.

EXAMPLE 57

69 was obtained using Method H H-NMR (300 MHz, CDCl₃): δ 6.60 (s, 1H); 6.48 (s, 1H); 6.40 (s, 1H); 5.97 (dd, 2H); 5.69 (s, 1H); 5.12 (d, 1H); 4.81 (s, 1H); 4.48 (d, 1H); 4.47-4-46 (m, 1H); 4.16 (d, 1H); 4.04 (dd, 1H); 3.84 (q, 2H); 3.79 (s, 3H); 3.61-3.54 (m, 1H); 3.58 (s, 3H); 3.22-3.18 (m, 1H); 3.18-3.09 (m, 1H); 2.88-2.84 (m, 2H); 2.86-2.78 (m, 1H); 2.68-2.58 (m, 1H); 2.52-2.44 (m, 1H); 2.39-2.12 (m, 2H); 2.32 (s, 3H); 2.26 (s, 3H); 2.17 (s, 3H); 2.02 (s, 3H); 1.80-1.73 (m, 2H); 0.96 (t, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.9, 147.9, 147.6, 147.0, 145.4, 143.1, 141.4, 140.7, 131.7, 128.5, 126.6, 121.9, 121.1, 116.0, 112.7, 111.1, 101.9, 82.3, 70.4, 64.8, 61.5, 60.5, 58.0, 57.8, 56.1, 55.4, 55.1, 42.3, 41.6, 39.9, 32.1, 28.8, 29.2, 24.2, 22.9, 22.5, 20.6, 16.0, 14.3, 10.6, 9.8.

ESI-MS m/z: Calcd. for C₄₂H₄₉N₃O₁₁S: 803.9 Found (M−H₂O+H⁺): 786.2.

EXAMPLE 58

70 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.60 (s, 1H); 6.48 (s, 1H); 6.40 (s, 1H); 6.03-5.94 (m, 1H); 5.97 (dd, 2H); 5.72 (s, 1H); 5.32 (dd, 1H); 5.21 (dd, 1H); 5.12 (d, 1H); 4.81 (s, 1H); 4.50-4.47 (m, 4H); 4.16 (d 1H); 4.04 (dd, 1H); 3.79 (s, 3H); 3.61 (d, 1H); 3.59 (s, 3H); 3.22-3.18 (m, 1H); 3.18-3.09 (m, 1H); 2.88-2.84 (m, 2H); 2.86-2.78 (m, 1H); 2.68-2.58 (m, 1H); 2.52-2.44 (m, 1H); 2.33-2.12 (m, 2H); 2.32 (s, 3H); 2.26 (s, 3H); 2.17 (s, 3H); 2.02 (s, 3H).

ESI-MS m/z: Calcd. for C₄₂H₄₇N₃O₁₁S: 801.2 Found (M−H₂O+H⁺): 784.2.

EXAMPLE 59

71 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 7.36-7.25 (m, 5H); 6.60 (s, 1H); 6.50 (s, 1H); 6.41 (s, 1H); 5.98 (dd, 2H); 5.69 (s, 1H); 5.12 (d, 1H); 5.02 (s, 2H); 4.81 (s, 1H); 4.48 (d, 1H); 4.48-4.46 (m, 1H); 4.16 (d 1H); 4.04 (dd, 1H); 3.78 (s, 3H); 3.60 (s, 3H); 3.22-3.18 (m, 1H); 3.18-3.09 (m, 1H); 2.88-2.84 (m, 2H); 2.86-2.78 (m, 1H); 2.64-2.58 (m, 1H); 2.46-2.40 (m, 1H); 2.34-2.12 (m, 2H); 2.31 (s, 3H); 2.26 (s, 3H); 2.17 (s, 3H); 2.03 (s, 3H).

ESI-MS m/z: Calcd. for C₄₆H₄₇N₃O₁₁S: 851.9 Found (M−H₂O+H⁺): 834.3.

EXAMPLE 60

Compound 11 (31%) was recovered after chromatographic purification.

72 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 7.31-7.20 (m, 5H); 6.60 (s, 1H); 6.55 (s, 1H); 6.53 (s, 1H); 6.00 (d, 1H); 5.93 (d, 1H); 5.70(s, 1H); 5.11 (d, 1H); 4.81 (s, 1H); 4.47 (d, 1H); 4.16 (d, 1H); 4.02 (dd, 1H); 3.79 (s, 3H); 3.58 (d, 1H); 3.50 (s, 3H); 3.21-3.08 (m, 2H); 3.02 (t, 2H); 2.87-2.80 (m, 5H); 2.66-2.44 (m, 3H); 2.36-2.22 (m, 1H); 2.31 (s, 3H); 2.27 (s, 3H); 2.17 (s, 3H); 2.01 (s, 3H).

ESI-MS m/z: Calcd. for C₄₈H₅₁N₃O₁₂S: 893.2 Found (M−H₂O+H⁺): 876.5.

EXAMPLE 61

73 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 6.61 (s, 1H); 6.60 (s, 1H); 6.57 (s, 1H); 6.00 (d, 1H); 5.93 (d, 1H); 5.73 (s, 1H); 5.11 (d, 1H); 4.82 (s, 1H); 4.84 (s, 2H); 4.17-4.15 (m, 1H); 4.03 (dd, 1H); 3.80 (t, 2H); 3.79 (s, 3H); 3.65-3.58 (m, 1H); 3.54 (s, 3H); 3.23-3.10 (m, 2H); 2.99 (t, 2H); 2.88-2.80 (m, 4H); 2.68-2.46 (m, 3H); 2.37-2.17 (m, 1H); 2.31 (s, 3H); 2.26 (s, 3H); 2.18 (s, 3H); 2.01 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.2, 168.6, 148.4, 147.9, 145.4, 143.2, 141.5, 140.7, 138.3, 133.3, 131.6, 129.8, 129.7, 129.5, 128.8, 122.5, 121.8, 121.1, 115.9, 112.0, 101.9, 82.3, 65.1, 61.6, 60.5, 58.0, 57.8, 56.1, 55.3, 55.1, 42.4, 41.5, 39.7, 39.0, 37.5, 29.9, 28.8, 27.1, 24.3, 20.6, 16.0, 9.9.

ESI-MS m/z: Calcd. for C₄₂H₄₆ClN₃O₁₂S: 851.2 Found (M−H₂O+H⁺): 834.2.

EXAMPLE 62

74 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 6.60 (s, 1H); 6.46 (s, 1H); 6.44 (s, 1H); 6.01 (d, 1H); 5.93 (d, 1H); 5.73 (s, 1H); 5.12 (d, 1H); 4.81 (s, 1H); 4.48 (s, 2H); 4.16 (d, 1H); 4.04 (dd, 1H); 3.78 (s, 3H); 3.60 (s, 3H); 3.58-3.56 (m, 1H); 3.22-3.08 (m, 2H); 2.93-2.75 (m, 3H); 2.65-2.44 (m, 2H); 2.37-2.14 (m, 1H); 2.31 (s, 3H); 2.25 (s, 3H); 2.17 (s, 3H); 2.02 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.7, 147.9, 145.3, 144.6, 144.4, 143.1, 141.4, 140.7, 131.7, 131.1, 129.4, 129.2, 129.0, 122.0, 121.1, 116.1, 114.2, 110.0, 101.8, 82.3, 65.7, 64.8, 61.5, 60.5, 58.0, 57.9, 56.1, 55.3, 55.1, 42.3, 41.6, 39.8, 29.9, 29.5, 29.0, 24.2, 22.9, 20.6, 19.4, 16.0, 14.3, 9.8.

ESI-MS m/z: Calcd. for C₄₃H₄₂F₇N₃O₁₂S: 957.2 Found (M−C₄F₇O−H₂O+2H⁺): 744.2.

EXAMPLE 63

75 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 7.08 (dd, 1H); 6.71 (s, 1H); 6.60 (s, 2H); 6.00 (d, 1H); 5.92 (d, 1H); 5.74 (s, 1H); 5.12 (d, 1H); 4.99 (dd, 1H); 4.81 (s, 1H); 4.63 (dd, 1H); 4.48 (d, 2H); 4.17 (dd, 1H); 3.79 (s, 3H); 3.60-3.57 (m, 1H); 3.57 (s, 3H); 3.24-3.22 (m, 1H); 3.17-3.09 (m, 1H); 2.93-2.78 (m, 3H); 2.68-2.46 (m, 2H); 3.37-2.22 (m, 1H); 2.31 (s, 3H); 2.26 (s, 3H); 2.17 (s, 3H); 2.01 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.1, 151.0, 148.4, 147.9, 145.4, 142.9, 141.5, 140.7, 138.5, 133.7, 131.6, 129.5, 128.9, 122.0, 121.8, 121.1, 118.0, 116.0, 112.2, 101.9, 98.7, 82.3, 65.1, 61.7, 60.5, 58.0, 57.8, 56.1, 55.4, 55.1, 42.2, 41.6, 39.7, 29.9, 28.8, 24.2, 20.6, 16.0, 9.8.

ESI-MS m/z: Calcd. for C₄₂H₄₅N₃O₁₃S: 831.2 Found (M−H₂O+H⁺): 814.2.

EXAMPLE 64

Compound 21 (17%) was recovered after chromatographic purification.

76 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 8.66 (s, 1H); 7.67-7.70 (m, 2H); 7.36-7.29(m, 2H); 6.74 (s, 1H); 6.60 (s, 2H); 5.99 (d, 1H); 5.92 (d, 1H); 5.76 (s, 1H); 5.13 (d, 1H); 4.81 (s, 1H); 4.47 (s, 2H); 4.15 (d, 1H); 4.04 (d, 1H); 3.78 (s, 3H); 3.57-3.56 (m, 1H); 3.54 (s, 3H); 3.47-3.44 (m, 1H); 3.21-3.10 (m, 2H); 2.92-2.79 (m, 3H); 2.70-2.48 (m, 2H); 2.38-2.19 (m, 1H); 2.31 (s, 3H); 2.27 (s, 3H); 2.16 (s, 3H); 2.01 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.2, 160.9, 156.5, 155.6, 150.0, 148.4, 147.9, 145.3, 143.1, 141.5, 140.7, 138.3, 134.9, 133.5, 131.7, 129.9, 129.4, 128.9, 125.1, 122.6, 121.9, 121.1, 118.2, 118.0, 117.4, 117.0, 116.0, 112.0, 101.9, 82.3, 65.2, 61.7, 60.5, 58.0, 57.9, 56.1, 55.4, 55.1, 42.4, 41.6, 39.7, 29.9, 28.8, 24.2, 20.6, 16.0, 9.8.

ESI-MS m/z: Calcd. for C₄₉H₄₇N₃O₁₄S: 933.2 Found (M−H₂O+H⁺): 916.3.

EXAMPLE 65

The reaction was performed with a mixture of compound 22 and 23 (3:1) using Method H, thus compounds 77 and 78 were isolated after chromatographic as pure compounds.

77: ¹H-NMR (300 MHz, CDCl₃): δ 7.44 (d, 1H); 6.61-6.51 (m, 5H); 6.19 (s, 1H); 6.00 (s, 1H); 5.92 (s, 1H); 5.73 (s, 1H); 5.10 (d, 1H); 4.79 (s, 1H); 4.45 (s, 2H); 4.15-4.14 (m, 1H); 4.01 (d, 1H); 3.85 (s, 2H); 3.78 (s, 3H); 3.57-3.56 (m, 1H); 3.49 (s, 3H); 3.21-3.00 (m, 3H); 3.04 (s, 6H); 2.86-2.78 (m, 3H); 2.64-2.43 (m, 2H); 2.30 (s, 3H); 2.25 (s, 3H); 2.16 (s, 3H); 2.00 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 171.9, 167.1, 161.6, 155.8, 152.9, 148.0, 147.9, 147.6, 145.1, 142.9, 141.2, 140.4, 138.1, 133.2, 131.5, 129.1, 128.6, 125.2, 122.0, 121.6, 120.8, 117.8, 115.7, 111.7, 110.7, 108.8, 108.4, 101.6, 98.3, 82.0, 64.9, 61.4, 60.3, 57.7, 55.9, 55.0, 54.8, 42.1, 41.3, 40.1, 39.4, 37.6, 29.6, 28.6, 24.0, 20.4, 15.7, 14.1, 9.6.

ESI-MS m/z: Calcd. for C₅₂H₅₄N₄O₁₄S: 990.3 Found (M−H₂O+H⁺): 973.3.

78: ¹H-NMR (300 MHz, CDCl₃): δ 7.69 (s, 1H); 7.51 (d, 1H); 7.45 (d, 1H); 6.92 (s, 1H); 6.61-6.48 (m, 5H); 6.33 (s, 1H); 6.21 (s, 1H); 6.19 (s, 1H); 6.01 (s, 1H); 5.94 (s, 1H); 5.08 (d, 1H); 4.74 (s, 1H); 4.47 (s, 1H); 4.32-4.28 (m, 2H); 4.04-3.94 (m, 3H); 3.85 (s, 2H); 3.67 (s, 3H); 3.61 (d, 1H); 3.47 (s, 3H); 3.26-2.80 (m, 5H); 3.05 (s, 6H); 2.97 (s, 6H); 2.60-2.42 (m, 2H); 2.29 (s, 6H); 2.19 (s, 3H); 2.06 (s, 3H).

ESI-MS m/z: Calcd. for C₆₅H₆₅N₅O₁₇S: 1220.3 Found (M+H⁺): 1221.3.

EXAMPLE 66

79 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.62 (s, 1H), 6.61 (s, 1H), 6.57 (s, 1H), 5.97 (d, 2H), 5.72 (s, 1H), 5.12 (d, 1H), 5.08 (bd, 1H), 4.82 (s, 1H), 4.55-4.44 (m, 3H), 4.17 (d, 1H), 4.03 (dd, 1H), 3.79 (s, 3H), 3.59 (d, 1H), 3.53 (s, 3H), 3.25-3.20 (m, 1H), 3.15-3.09 (m, 1H), 2.92-2.78 (m, 3H), 2.67-2.59 (m, 1H), 2.52-2.47 (m, 1H), 2.37-2.18 (m, 2H), 2.32 (s, 3H), 2.27 (s, 3H), 2.18 (s, 3H), 2.02 (s, 3H), 1.50 (d, 3H), 1.44 (s, 9H).

ESI-MS m/z: Calcd. for C₄₇H₅₆N₄O₁₄S: 932.3 Found (M−H₂O+H⁺): 915.3.

EXAMPLE 67

Compound 6 (42%) was recuperatd after chromatographic purification.

80 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.96 (s, 1H), 6.61 (s, 1H), 6.54 (s, 1H), 5.98 (dd, 2H), 5.12 (d, 1H), 4.83 (s, 1H), 4.49 (d, 1H), 4.33 (bs, 1H), 4.03 (dd, 1H), 3.78 (s, 3H), 3.70 (d, 1H), 3.60 (d, 1H), 3.55 (s, 3H), 3.29-3.24 (m, 1H), 3.18-3.09 (m, 1H), 3.03-2.80 (m, 3H), 2.69-2.59 (m, 1H), 2.53-2.05 (m, 1H), 2.42-2.13 (m, 2H), 2.37 (s, 3H), 2.33 (s, 3H), 2.31 (s, 3H), 2.24 (s, 3H), 2.13 (s, 3H), 2.03 (s, 3H).

ESI-MS m/z: Calcd. for C₄₃H₄₇N₃O₁₃S: 845.3 Found (M+H⁺): 846.3.

EXAMPLE 68

Compound 9 was recovered (25%) after chromatographic purification.

81 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.95 (s, 1H); 6.59 (s, 2H); 6.54 (d, 1H); 6.01 (dd, 1H); 5.94 (dd, 2H); 5.12 (d, 1H); 4.81 (s, 1H); 4.49 (d, 1H); 4.34 (s, 1H); 4.02 (dd, 1H); 3.75 (s, 3H); 3.67 (d, 1H); 3.58 (d, 1H); 3.53 (s, 3H); 3.25-3.23 (m, 1H); 3.17-3.12 (m, 1H); 2.92-2.80 (m, 3H); 2.69-2.63 (m, 1H); 2.60 (t, 2H); 2.54-2.50 (m, 1H); 2.48 (t, 2H); 2.32 (s, 3H); 2.29 (s, 3H); 2.13 (s, 3H); 2.03 (s, 3H); 1.91-1.80 (m, 2H); 1.79-1.68 (m, 2H); 1.09 (t, 3H); 1.00 (t, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.1, 171.9, 171.4, 148.6, 148.0, 145.5, 143.7, 141.4, 140.8, 138.8, 132.7, 131.6, 131.5, 128.8, 127.6, 124.5, 122.6, 121.7, 116.0, 111.9, 102.0, 82.0, 65.2, 61.5, 60.3, 57.9, 57.8, 56.4, 56.2, 55.2, 42.6, 41.6, 39.8, 36.3, 36.0, 29.9, 29.5, 28.8, 24.2, 20.5, 18.9, 18.7, 16.0, 14.0, 13.7, 9.8.

ESI-MS m/z: Calcd. for C₄₇H₅₅N₃O₁₃S: 901.3 Found (M−H₂O+H⁺): 884.5.

EXAMPLE 69

82 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.95 (s, 1H); 6.59 (s, 1H); 6.54 (s, 1H); 6.02 (d, 1H); 5.94 (s, 1H); 5.12 (d, 1H); 4.81 (s, 1H); 4.49 (s, 1H); 4.35 (s, 1H); 4.02 (d, 1H); 3.75 (s, 3H); 3.68-3.67 (m, 1H); 3.58-3.56(m, 1H); 3.53 (s, 3H); 3.26-3.24 (m, 1H); 3.14-3.08 (m, 1H); 2.92-2.80 (m, 3H); 2.61 (t, 2H); 2.49 (t, 2H); 2.32 (s, 3H); 2.29 (s, 3H); 2.13 (s, 3H); 2.03 (s, 3H); 1.83-1.59 (m, 4H); 1.42-1.14 (m, 20H).

ESI-MS m/z: Calcd. for C₅₅H₇₁N₃O₁₃S: 1013.4 Found (M−H₂O+H⁺): 996.5.

EXAMPLE 70

83 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.95 (s, 1H); 6.59 (s, 1H); 6.54 (s, 1H); 5.98 (dd, 2H); 5.12 (d, 1H); 4.81 (s, 1H); 4.48 (d, 1H); 4.47-4.45 (m, 1H); 4.17 (d, 1H); 4.01 (dd, 1H); 3.75 (s, 3H); 3.66 (d, 1H); 3.59-3.56(m, 1H); 3.53 (s, 3H); 3.26-3.21 (m, 1H); 3.18-3.09 (m, 1H); 2.93-2.90 (m, 2H); 2.86-2.78 (m, 1H); 2.69-2.58 (m, 1H); 2.61(t, 2H); 2.52-2.44 (m, 1H); 2.49 (t, 2H); 2.37-2.12 (m, 2H); 2.31 (s, 3H); 2.29 (s, 3H); 2.12 (s, 3H); 2.03 (s, 3H); 1.84-1.80 (m, 2H); 1.71-1.64(m, 2H); 1.40-1.17 (m, 54H).

EXAMPLE 71

84 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 7.94 (d, 1H); 7.81 (d, 1H); 7.61-7.53 (m, 4H); 7.45-7.39 (m, 6H); 6.99 (s, 1H); 6.67 (d, 1H); 6.66 (d, 1H); 6.60 (s, 1H); 6.57 (d, 1H); 6.02 (s, 1H); 5.94 (d, 1H); 5.15 (d, 1H); 4.83 (s, 1H); 4.51 (d, 1H); 4.48-4.46 (m, 1H); 4.05 (dd, 1H); 3.79 (s, 3H); 3.62-3.61 (m, 1H); 3.56 (s, 3H); 3.27-3.16 (m, 1H); 2.96-2.88 (m, 3H); 2.70-2.50 (m, 2H); 2.43-2.39 (m, 2H); 2.35 (s, 3H); 2.234 (s, 3H); 2.17 (s, 3H); 2.05 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 164.9, 164.5, 148.5, 148.0, 146.8, 146.5, 145.3, 143.4, 141.2, 140.6, 138.5, 134.2, 134.0, 131.4, 130.8, 130.5, 129.0, 128.9, 128.7, 128.2, 127.5, 125.0, 124.4, 122.5, 116.9, 115.8, 111.7, 101.7, 81.7, 67.6, 65.0, 61.2, 60.2, 57.7, 56.0, 55.1, 42.5, 41.4, 39.6, 32.6, 31.9, 29.6, 26.3, 28.6, 23.9, 22.6, 20.4, 15.8, 14.1, 9.6.

ESI-MS m/z: Calcd. for C₅₇H₅₅N₃O₁₃S: 1021.4 Found (M−H₂O+H⁺): 1004.6.

EXAMPLE 72

85 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 7.41-7.34 (m, 10H); 6.95 (s, 1H); 6.69 (s, 1H); 6.54 (s, 1H); 6.01 (d, 1H); 5.93 (s, 1H); 5.35-5.25(m, 2H); 5.11 (d, 1H); 4.80 (s, 1H); 4.47 (s, 1H); 4.32 (s, 1H); 4.03 (dd, 1H); 3.75 (s, 3H); 3.52 (s, 3H); 3.24 (s, 1H); 3.14-3.06 (m, 1H); 2.90-2.78 (m, 3H); 2.66-2.45 (m, 2H); 2.31 (s, 3H); 2.26-2.16 (m, 2H); 2.20 (s, 3H); 2.09 (s, 3H); 2.02 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.1, 153.5, 153.2, 148.5, 148.0, 145.5, 144.1, 141.5, 140.7, 139.0, 135.2, 135.1, 133.1, 131.6, 128.9, 128.8, 128.8, 128.7, 128.6, 128.4, 127.7, 122.2, 115.8, 112.0, 101.9, 82.0, 70.6, 70.5, 65.3, 61.6, 60.4, 57.8, 56.2, 55.9, 55.3, 42.4, 41.5, 39.7, 31.8, 29.9, 28.8, 24.1, 22.8, 20.3, 15.9, 14.3, 9.8.

ESI-MS m/z: Calcd. for C₅₅H₅₅N₃O₁₅S: 1029.3 Found (M−H₂O+H⁺): 1012.4.

EXAMPLE 73

86 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.92 (s, 1H); 6.69 (s, 1H); 6.55 (s, 1H); 5.97 (dd, 2H); 5.12 (d, 1H); 4.81 (s, 1H); 4.49 (d, 1H); 4.33 (s, 1H); 4.03 (dd, 1H); 3.80 (s, 3H); 3.60-3.56 (m, 1H); 3.57 (s, 3H); 3.26-3.24 (m, 1H); 3.16-3.06 (m, 1H); 2.90-2.89 (m, 2H); 2.88-2.78 (m, 1H); 2.69-2.58 (m, 1H); 2.53-2.44 (m, 1H); 2.34-2.26 (m, 2H); 2.33 (s, 3H); 2.31 (s, 3H); 2.14 (s, 3H); 2.04 (s, 3H); 1.53 (s, 9H); 1.50 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.2, 151.8, 151.4, 148.7, 148.1, 145.5, 141.2, 141.5, 140.8, 139.0, 132.8, 131.3, 128.9, 127.3, 124.4, 122.4, 121.9, 116.0, 112.1, 101.9, 83.5, 83.2, 82.0, 65.4, 61.5, 60.2, 57.9, 56.3, 56.0, 55.4, 42.4, 41.6, 39.5, 29.9, 28.9, 27.8, 27.7, 24.1, 20.3, 15.9, 14.3, 9.7.

ESI-MS m/z: Calcd. for C₄₉H₅₉N₃O₁₅S: 961.4 Found (M−H₂O+H⁺) 944.4.

EXAMPLE 74

87 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.76 (s, 1H); 6.45 (s, 1H); 6.39 (s, 1H); 6.02 (d, 1H); 5.93 (d, 1H); 5.13 (d, 1H); 4.81 (s, 1H); 4.49 (d, 1H); 4.36 (s, 1H); 4.18(d, 1H); 4.11(d, 1H); 4.03(d, 1H); 3.90 (s, 3H); 3.81 (s, 3H); 3.75 (s, 3H); 3.58 (s, 3H); 3.58-3.56(m, 1H); 3.23-3.11 (m, 2H); 2.94-2.81 (m, 3H); 2.71-2.61 (m, 1H); 2.53-2.47(m, 1H); 2.35-2.27 (m, 1H); 2.27 (s, 3H); 2.22 (s, 3H); 2.16 (s, 3H); 2.01 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.7, 151.8, 148.7, 148.0, 146.6, 145.4, 141.4, 140.7, 131.4, 131.3, 128.5, 126.6, 124.6, 124.4, 122.0, 116.1, 111.2, 110.6, 101.9, 81.7, 64.9, 61.3, 60.2, 59.6, 58.0, 57.9, 56.2, 55.9, 55.3, 55.2, 42.3, 41.7, 39.9, 31.8, 29.9, 29.2, 24.3, 22.8, 20.4, 16.0, 14.3, 9.8.

ESI-MS m/z: Calcd. for C₄₁H₄₇N₃O₁₁S: 789.2 Found (M−H₂O+H⁺): 772.2.

EXAMPLE 75

88 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.77 (s, 1H); 6.46 (s, 1H); 6.40 (s, 1H); 5.97 (dd, 2H); 5.13 (d, 1H); 4.81 (s, 1H); 4.49 (d, 1H); 4.39 (s, 1H); 4.10 (d 1H); 4.03 (dd, 1H); 3.99 (q, 2H); 3.96 (q, 2H); 3.83 (s, 3H); 3.61-3.54 (m, 1H); 3.58 (s, 3H); 3.24-3.18 (m, 1H); 3.18-3.09 (m, 1H); 2.88-2.85 (m, 2H); 2.86-2.78 (m, 1H); 2.69-2.58 (m, 1H); 2.54-2.44 (m, 1H); 2.35-2.12 (m, 2H); 2.28 (s, 3H); 2.25 (s, 3H); 2.17 (s, 3H); 2.03 (s, 3H); 1.40 (t, 3H); 1.36 (t, 3H).

ESI-MS m/z: Calcd. for C₄₃H₅₁N₃O₁₁S: 817.3 Found (M−H₂O+H⁺): 800.3.

EXAMPLE 76

89 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.79 (s, 1H); 6.48 (s, 1H); 6.40 (s, 1H); 5.98 (dd, 2H); 5.13 (d, 1H); 4.81 (s, 1H); 4.48 (d, 1H); 4.42 (s, 1H); 4.10 (d, 1H); 4.04 (dd, 1H); 3.86 (q, 2H); 3.84 (q, 2H); 3.79 (s, 3H); 3.60 (s, 3H); 3.60-3.58 (m, 1H); 3.24-3.18 (m, 1H); 3.18-3.09 (m, 1H); 2.88-2.84 (m, 2H); 2.86-2.78 (m, 1H); 2.68-2.58 (m, 1H); 2.52-2.44 (m, 1H); 2.39-2.12 (m, 2H); 2.28 (s, 3H); 2.25 (s, 3H); 2.18 (s, 3H); 2.02 (s, 3H); 1.84-1.74 (m, 4H); 1.10 (t, 3H); 0.96 (t, 3H).

ESI-MS m/z: Calcd. for C₄₅H₅₅N₃O₁₁S: 845.3 Found (M−H₂O+H⁺): 828.0.

EXAMPLE 77

90 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.79 (s, 1H); 6.47 (s, 1H); 6.40 (s, 1H); 6.16-5.92 (m, 2H); 5.97 (dd, 2H); 5.45 (dd, 1H); 5.31 (dd, 1H); 5.24 (dd, 1H); 5.50 (dd, 1H); 5.12 (d, 1H); 4.80 (s, 1H); 4.78 (dd, 1H); 4.49 (d, 2H); 4.30 (s, 1H); 4.35 (dd, 1H); 4.11 (d, 1H); 4.04 (dd, 1H); 3.83 (s, 3H); 3.59 (s, 3H); 3.59-3.58 (m, 1H); 3.24-3.18 (m, 1H); 3.18-3.09 (m, 1H); 2.90-2.88 (m, 2H); 2.88-2.78 (m, 1H); 2.68-2.58 (m, 1H); 2.52-2.44 (m, 1H); 2.37-2.12 (m, 2H); 2.28 (s, 3H); 2.23 (s, 3H); 2.16 (s, 3H); 2.02 (s, 3H).

ESI-MS m/z: Calcd. for C₄₅H₅₁N₃O₁₁S: 841.3 Found (M−H₂O+H⁺): 824.3.

EXAMPLE 78

91 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 7.48-7.25 (m, 10H); 6.82 (s, 1H); 6.48 (s, 1H); 6.41 (s, 1H); 5.98 (dd, 2H); 5.32 (d, 1H); 5.12 (d, 1H); 5.02 (s, 2H); 4.84 (d, 1H); 4.80 (s, 1H); 4.48 (d, 1H); 4.45 (s, 1H); 4.50-4.00 (m, 2H); 3.85 (s, 3H); 3.61-3.57 (m, 1H); 3.60 (s, 3H); 3.24-3.18 (m, 1H); 3.18-3.09 (m, 1H); 2.88-2.84 (m, 2H); 2.86-2.78 (m, 1H); 2.64-2.58 (m, 1H); 2.46-2.40 (m, 1H); 2.36-2.12 (m, 2H); 2.30 (s, 3H); 2.03 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.6, 150.5, 149.1, 147.3, 145.4, 141.4, 140.7, 138.4, 137.3, 131.4, 131.3, 128.7, 128.6, 128.5, 128.1, 128.0, 127.9, 127.3, 125.1, 124.9, 122.1, 116.2, 116.1, 113.9, 11.3, 101.8, 82.0, 74.2, 71.0, 64.9, 61.4, 59.8, 58.1, 58.0, 56.2, 55.7, 55.4, 42.4, 42.2, 41.5, 39.8, 29.9, 29.1, 24.3, 20.1, 16.0, 9.8.

ESI-MS m/z: Calcd. for C₅₃H₅₅N₃O₁₁S: 941.4 Found (M−H₂O+H⁺): 924.3.

EXAMPLE 79

Compound 30 (15%) was recovered after chromatographic purification.

92 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 7.17 (dd, 1H); 7.08 (dd, 1H); 6.96 (s, 1H); 6.72 (s, 1H); 6.58 (s, 1H); 6.02 (d, 1H); 5.94 (d, 1H); 5.12 (d, 1H); 4.99 (dd, 2H); 4.82 (s, 1H); 4.69 (dd, 1H); 4.63 (dd, 1H); 4.50-4.48 (m, 1H); 4.39-4.37 (m, 1H); 4.05 (dd, 1H); 3.84-3.79 (m, 1H); 3.80 (s, 3H); 3.61-3.59 (m, 1H); 3.58 (s, 3H); 3.29-3.26 (m, 1H); 3.18-3.09 (m, 1H); 2.93-2.80 (m, 3H); 2.70-2.47 (m, 2H); 2.53 (s, 3H); 2.33 (s, 3H); 2.30-2.24 (m, 1H); 2.15 (s, 3H); 2.04 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.1, 168.8, 151.0, 150.8, 148.4, 147.9, 145.5, 143.8, 143.1, 142.9, 141.5, 140.8, 138.5, 133.5, 131.8, 129.0, 128.1, 124.2, 122.1, 121.6, 115.8, 112.8, 112.2, 102.0, 98.7, 82.0, 65.3, 61.6, 60.6, 57.8, 56.2, 56.0, 55.3, 42.5, 41.5, 39.7, 29.9, 28.9, 24.1, 20.4, 15.9, 9.8.

ESI-MS m/z: Calcd. for C₄₅H₄₇N₃O₁₅S: 901.2 Found (M−H₂O+H⁺): 884.3.

EXAMPLE 80

93 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.47 (s, 1H), 6.44 (s, 1H), 6.19 (s, 1H), 5.98 (dd, 2H), 5.70 (bp, 1H), 5.01 (d, 1H), 4.83 (d, 1H), 4.48 (bp, 1H), 4.42 (d, 1H), 4.14 (dd, 1H), 3.79 (s, 3H), 3.78 (dd, 1H), 3.58 (d, 1H), 3.53 (s, 3H), 3.23-3.20 (m, 2H), 2.91-2.70 (m, 2H), 2.63-2.47 (m, 5H), 2.30 (s, 3H), 2.23 (s, 6H), 2.15 (s, 3H), 2.01 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 168.7, 147.4, 145.4, 144.4, 144.1, 142.6, 141.7, 140.8, 131.3, 129.6, 129.1, 127.1, 122.1, 121.3, 118.0, 116.1, 113.8, 111.6, 110.5, 101.7, 83.2, 71.2, 62.5, 60.1, 59.2, 57.7, 55.3, 54.9, 49.0, 43.1, 42.1, 41.6, 38.9, 28.5, 24.8, 20.3, 15.6, 9.7.

ESI-MS m/z: Calcd. for C₄₀H₄₅N₃O₁₁S: 775.3. Found (M+H⁺): 776.1.

EXAMPLE 81

94 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.48 (s, 1H), 6.44 (s, 1H), 6.21 (s, 1H), 5.98 (d, 2H), 5.69 (bs, 1H), 4.99 (d, 1H), 4.87 (d, 1H), 4.50-4.44 (m, 2H), 4.17-4.12 (m, 1H), 3.89-3.84 (m 1H), 3.80 (s, 3H), 3.58-3.55 (m, 1H), 3.55 (s, 3H), 3.26-3.22 (m, 1H), 3.02-2.42 (m, 6H), 2.37-2.02 (m, 4H), 2.31 (s, 3H), 2.28 (s, 3H), 2.12 (s, 3H), 2.05 (s, 3H), 0.88 (t, 3H).

ESI-MS m/z: Calcd. for C₄₁H₄₇N₃O₁₁S: 789.3. Found (M−H₂O+H⁺): 772.3.

EXAMPLE 82

Compound 32 was recovered after chromatographic purification (15%).

95 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 7.05 (dd, 1H); 6.48 (s, 1H); 6.46 (s, 1H); 6.15 (s, 1H); 6.03 (s, 1H); 5.92 (s, 1H); 5.73 (s, 1H); 4.91 (dd, 1H); 4.83 (s, 1H); 4.72 (dd, 1H); 4.45-4.48 (m, 3H); 4.13 (d, 1H); 4.01-3.94 (m, 2H); 3.81 (s, 3H); 3.71-3.66 (m, 2H); 3.59 (s, 3H); 3.23-3.20 (m, 3H); 2.83-2.81 (m, 2H); 2.72-2.62 (m, 1H); 2.54-2.42 (m, 2H); 2.33 (s, 3H); 2.22 (s, 3H); 2.14 (s, 3H); 2.02 (s, 3H).

ESI-MS m/z: Calcd. for C₄₂H₄₅N₃O₁₃S: 831.3. Found (M−H₂O+H⁺): 814.2.

EXAMPLE 83

96 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 7.00 (bs, 1H), 6.49 (s, 1H), 6.42 (bs, 1H), 6.00 (dd, 2H), 5.40 (bs, 1H), 5.12 (d, 1H), 4.84-3.69 (m, 4H), 3.84-3.50 (m, 5H), 3.50 (s, 3H), 3.24-2.57 (m, 7H), 2.42-2.13 (m, 2H), 2.40 (s, 3H), 2.33 (s, 3H), 2.29 (s, 3H), 2.13 (s, 3H), 2.03 (s, 3H).

ESI-MS m/z: Calcd. for C₄₁H₄₅N₃O₁₂S: 803.3 Found (M−H₂O+H⁺): 804.

EXAMPLE 84

97 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.93 (s, 1H); 6.47 (s, 1H); 6.42 (s, 1H); 5.98 (dd, 2H); 5.13 (d, 1H); 4.81 (s, 1H); 4.50 (d, 1H); 4.36 (s, 1H); 4.05 (dd, 1H); 3.79 (s, 3H); 3.62-3.58 (m, 1H); 3.61 (s, 3H); 3.27-3.24 (m, 1H); 3.18-3.06 (m, 1H); 2.91-2.89 (m, 2H); 2.86-2.78 (m, 1H); 2.68-2.56 (m, 1H); 2.52-2.44 (m, 1H); 2.33-2.12 (m, 2H); 2.32 (s, 3H); 2.31 (s, 3H); 2.14 (s, 3H); 2.04 (s, 3H); 1.53 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.6, 151.4, 148.1, 145.4, 144.6, 144.4, 144.2, 141.5, 140.0, 131.4, 131.3, 129.4, 127.3, 126.1, 124.4, 122.1, 116.0, 114.2, 110.0, 101.8, 83.2, 82.0, 65.1, 61.4, 60.2, 57.9, 56.3, 56.1, 55.3, 42.4, 41.3, 39.8, 32.1, 30.6, 29.9, 29.5, 29.0, 27.8, 24.1, 22.8, 20.3, 15.5, 14.2, 9.8.

ESI-MS m/z: Calcd. for C₄₄H₅₁N₃O₁₃S: 861.2 Found (M−H₂O+H⁺): 844.2.

EXAMPLE 85

Compound 36 (11%) was recovered after chromatographic purification.

98 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ d 6.77 (s, 1H), 6.47 (s, 1H), 6.42 (s, 1H), 5.98 (dd, 2H), 5.40 (bp, 1H), 5.13 (d, 1H), 4.81 (s, 1H), 4.49 (bs, 1H), 4.37 (bp, 1H), 4.11 (d, 1H), 4.03 (dd, 1H), 3.91 (s, 3H), 3.82 (s, 3H), 3.60 (s, 3H), 3.58-3.56 (m, 1H), 3.23-3.21 (m, 1H), 3.16-3.09 (m, 1H), 2.95-2.79 (m, 3H), 2.67-2.57 (m, 1H), 2.50-2.45 (m, 1H), 2.34-2.13 (m, 2H), 2.28 (s, 3H), 2.23 (s, 3H), 2.17 (s, 3H), 2.03 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.5, 168.1, 151.6, 148.5, 145.1, 144.4, 144.2, 141.2, 140.5, 131.2, 131.0, 129.1, 126.0, 124.5, 124.2, 122.0, 115.9, 114.0, 109.8, 101.6, 81.7, 64.8, 61.1, 60.0, 59.4, 57.8, 57.7, 56.0, 55.1, 55.1, 42.2, 42.2, 41.5, 39.6, 28.8, 24.1, 20.2, 15.8, 9.6.

ESI-MS m/z: Calcd. for C₄₀H₄₅N₃O₁₁S: 775.8 Found (M−H₂O+H⁺): 758.7.

EXAMPLE 86

99 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 7.18 (dd, 1H); 7.08 (dd, 1H); 7.04 (dd, 1H); 6.87 (s, 1H); 6.73 (s, 1H); 6.31 (s, 1H); 6.04 (d, 1H); 5.91 (d, 1H); 5.01 (dd, 1H); 4.99 (dd, 1H); 4.92 (d, 1H); 4.83 (s, 1H); 4.75 (d, 1H); 4.69-4.63 (m, 2H); 4.45-4.42 (m, 2H); 4.01-3.96 (m, 2H); 3.84 (s, 3H); 3.81-3.89 (m, 1H); 3.60-3.57 (m, 1H); 3.55 (s, 3H); 3.37-3.25 (m, 2H); 2.90-2.87 (m, 2H); 2.77-2.67 (m, 1H); 2.53-2.28 (m, 3H); 2.41 (s, 3H); 2.23 (s, 3H); 2.12 (s, 3H); 2.03 (s, 3H).

ESI-MS m/z: Calcd. for C₄₈H₄₉N₃O₁₇S: 971.2 Found (M−H₂O+H⁺): 954.3.

EXAMPLE 87

100 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 7.08 (dd, 1H); 7.04 (dd, 1H); 6.72 (s, 1H); 6.49 (s, 1H); 6.34 (s, 1H); 6.04 (s, 1H); 5.91 (s, 1H); 5.73 (s, 1H); 5.00 (dd, 1H); 4.93 (dd, 1H); 4.83 (s, 1H); 4.73 (d, 1H); 4.64 (dd, 1H); 4.51 (s, 1H); 4.44-4.40 (m, 2H); 4.14 (d, 1H); 4.07-4.01 (m, 1H); 3.96 (dd, 1H); 3.81 (s, 3H); 3.58-3.49 (m, 2H); 3.55 (s, 3H); 3.35-3.20 (m, 2H); 2.81 (d, 2H); 2.76-2.66 (m, 1H); 2.56-2.46 (m, 2H); 2.33 (s, 3H); 2.22 (s, 3H); 2.14 (s, 3H); 2.01 (s, 3H).

ESI-MS m/z: Calcd. for C₄₅H₄₇N₃O₁₅S: 901.9 Found (M−H₂O+H⁺): 884.2.

EXAMPLE 88

Compound 52 (19%) was recovered after chromatographic purification.

101 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.48 (s, 1H); 6.44 (s, 1H); 6.03 (d, 1H); 5.93 (d, 1H); 5.39 (s, 1H); 5.01 (d, 1H); 4.72 (s, 1H); 4.41-4.39 (m, 2H); 4.11-3.99 (m, 3H); 4.10 (s, 3H); 3.64-3.61 (m, 1H); 3.61 (s, 3H); 3.26-3.06 (m, 3H); 2.81-2.29 (m, 8H); 2.23 (s, 3H); 2.18 (s, 3H); 2.05 (s, 3H); 2.03 (s, 3H).

ESI-MS m/z: Calcd. for C₃₉H₄₁N₃O₁₂S: 775.2 Found (M+Na⁺): 798.2.

EXAMPLE 89

102 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 6.77 (s, 1H), 6.46 (s, 1H), 6.44 (s, 1H), 6.01 (d, 1H), 5.94 (d, 1H); 5.13 (d, 1H), 4.89-4.80 (m, 1H); 4.80 (s, 1H), 4.48 (d, 1H); 4.42 (s, 1H), 4.21 (d, 1H), 4.05 (dd, 1H), 3.81 (s, 3H), 3.61 (s, 3H), 3.55 (d, 1H), 3.20 (s, 1H), 3.16-3.08 (m, 1H), 2.89-2.86 (m, 2H), 2.80-2.76 (m, 1H), 2.64-2.47 (m, 2H); 2.32-2.12 (m, 2H); 2.28 (s, 3H), 2.25 (s, 3H), 2.20 (s, 3H), 2.03 (s, 3H); 1.45 (d, 3H); 1.14 (d, 3H). ¹³C-NMR (75 MHz, CDCl₃): δ 172.7, 168.5, 149.3, 148.8, 145.2, 144.6, 144.4, 141.3, 140.7, 135.8, 131.1, 129.2, 128.6, 126.3, 124.3, 116.1, 114.2, 109.9, 101.8, 81.9, 73.3, 64.9, 61.2, 59.1, 58.2, 58.1, 56.2, 55.3, 42.2, 42.1, 41.7, 39.6, 31.8, 29.9, 29.0, 24.2, 23.8, 22.8, 20.5, 16.0, 14.3, 9.8. ESI-MS m/z: Calcd. for C₄₂H₄₉N₃O₁₁S: 803.4 Found (M+H⁺): 804.4.

EXAMPLE 90

Method I: To a solution of 1 equiv. of compound 3 in THF/H₂O 4.5:0.5 (0.0052M) were added 5 equiv. of CuBr. After 24 h the reaction was quenched with NaHCO₃, diluted and extracted with CH₂Cl₂. The organic layer was dried with Na₂SO₄. Chromatography gives pure compound 104 (50%).

104 was obtained using Method I ¹H-NMR (300 MHz, CDCl₃): δ 6.47 (s, 2H); 6.45 (s, 1H); 5.98 (dd, 2H); 5.68 (s, 1H); 4.87 (s, 1H); 4.77 (d, 1H); 4.57 (s, 1H); 4.45 (d, 1H); 4.15 (d, 1H); 4.05 (dd, 1H); 3.79 (s, 3H); 3.64 (d, 1H); 3.58 (s, 3H); 3.25-3.20 (m, 2H); 2.80-2.82 (m, 3H); 2.67-2.63 (m, 2H); 2.52-2.44 (m, 1H); 2.32-2.12 (m, 2H); 2.31 (s, 3H); 2.24 (s, 3H); 2.12 (s, 3H); 2.02 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 168.9, 148.3, 147.6, 145.1, 141.2, 140.4, 139.1, 138.4, 131.4, 130.8, 128.7, 128.6, 122.9, 122.3, 121.6, 120.9, 120.6, 115.8, 111.7, 101.6, 82.0, 64.9, 61.4, 60.3, 57.8, 57.6, 55.9, 55.0, 54.9, 42.1, 41.3, 39.5, 29.6, 24.0, 20.5, 15.7, 9.6.

ESI-MS m/z: Calcd. for C₄₁H₄₂F₃N₃O₁₂S: 857.8 Found (M−H₂O+H⁺): 840.2.

EXAMPLE 91

To a solution of compound 4 in THF/H₂O 3:1 (0.027M) were added 15 equiv. of KOH. The reaction mixture was stirred at room temperature for 5 h. After this time the reaction was quenched with NaCl or diluted aqueous solution of HCl, extracted with CH₂Cl₂. The organic layer was dried with Na₂SO₄. Chromatography gives pure compound 106.

106. ¹H-NMR (300 MHz, CDCl₃): δ 6.70 (s, 1H); 6.61 (s, 1H); 6.53 (s, 1H); 5.92 (dd, 2H); 5.84 (s, 1H); 5.41 (s, 1H); 4.97 (d, 1H); 4.48 (d, 1H); 4.34 (s, 1H); 4.31 (dd, 1H); 4.16 (d 1H); 4.03 (dd, 1H); 3.80 (s, 3H); 3.59 (d, 1H); 3.55 (s, 3H); 3.43-3.40 (m, 1H); 3.18-3.08 (m, 1H); 2.95-2.93 (m, 2H); 2.81-2.75 (m, 1H); 2.69-2.58 (m, 1H); 2.45-2.24 (m, 2H); 2.34 (s, 3H); 2.19 (s, 3H); 2.15 (s, 3H); 1.50 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 171.7, 148.6, 148.0, 146.2, 146.0, 143.1, 139.0, 136.1, 132.4, 130.7, 129.4, 128.7, 122.4, 122.7, 118.2, 118.1, 113.1, 111.6, 101.2, 83.5, 64.4, 60.9, 60.7, 60.4, 59.8, 59.3, 55.2, 54.7, 54.6, 51.7, 43.1, 41.5, 39.5, 30.1, 29.8, 29.7, 28.6, 27.6, 25.5, 24.2, 15.9, 8.7.

ESI-MS m/z: Calcd. for C₄₃H₄₈N₄O₁₁S: 828.9 Found (M+H⁺):829.3.

EXAMPLE 92

Method A: To a solution of 1 equiv. of compound 106 in CH₂Cl₂ (0.032M) under Argon were added 2 equiv. of the anhydride and 2 equiv. of pyridine. The reaction was followed by TLC and quenched with NaHCO₃, extracted with CH₂Cl₂ and the organic layers dried with Na₂SO₄. Flash chromatography gives pure compounds.

107 was obtained using Method A. ¹H-NMR (300 MHz, CDCl₃): δ 6.70 (s, 1H); 6.59 (s, 1H); 6.58 (s, 1H); 6.04 (dd, 2H); 5.69 (s, 1H); 5.02 (d, 1H); 4.58 (s, 1H); 4.34 (s, 1H); 4.29 (dd, 1H); 4.21 (d 1H); 4.13 (dd, 1H); 3.76 (s, 3H); 3.59 (s, 3H); 3.50 (dd, 1H); 3.44-3.41 (m, 1H); 3.19-3.10 (m, 1H); 2.94 (d, 2H); 2.81-2.73 (m, 1H); 2.69-2.58 (m, 1H); 2.54-2.46 (m, 1H); 2.34-2.04 (m, 2H); 2.31 (s, 3H); 2.20 (s, 3H); 2.06 (s, 3H); 1.50 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 168.0, 157.9, 151.7, 149.0, 148.2, 145.8, 143.4, 141.4, 139.4, 130.7, 122.7, 120.7, 118.1, 117.8, 114.7, 113.1, 112.0, 102.5, 97.6, 83.7, 64.7, 61.3, 60.4, 60.0, 59.4, 55.7, 54.8, 54.6, 41.8, 41.7, 39.6, 32.1, 29.9, 29.5, 27.8, 24.1, 20.8, 16.0, 14.3, 9.4.

ESI-MS m/z: Calcd. for C₄₅H₄₇F₃N₄O₁₂S: 924.3 Found (M+H⁺): 925.3.

EXAMPLE 93

108 was obtained using Method A. ¹H-NMR (300 MHz, CDCl₃): δ 6.69 (s, 1H); 6.60 (s, 1H); 6.58 (s, 1H); 6.03 (d, 1H); 5.96 (d, 1H); 5.69 (s, 1H); 5.00 (d, 1H); 4.68 (s, 1H); 4.29-4.27 (m, 2H); 4.16-4.09 (m, 2H); 3.78 (s, 3H); 3.59 (s, 3H); 3.50 (d, 1H); 3.41 (s, 1H); 3.15-3.06 (m, 1H); 2.98-2.94 (m, 2H); 2.80-2.74 (m, 1H); 2.69-2.59 (m, 1H); 2.50-2.45 (m, 1H); 2.37-2.21 (m, 2H); 2.31 (s, 3H); 2.18 (s, 3H); 2.08 (s, 3H); 1.51 (s, 9H); 1.47 (s, 9H).

ESI-MS m/z: Calcd. for C₄₈H₅₆N₄O₁₃S: 928.4 Found (M+H⁺): 929.3.

EXAMPLE 94

If the acylation reaction of compound 106 is performed with TEA (10 equiv.) as base instead of pyridine compound 109 is obtained (Method A).

109. ¹H-NMR (300 MHz, CDCl₃): δ 6.89 (s, 1H); 6.72 (s, 1H); 6.18 (s, 1H); 6.16 (d, 1H); 6.04 (d, 1H); 4.76 (d, 1H); 4.54 (s, 1H); 4.41 (s, 1H); 4.12 (d, 1H); 4.08 (dd, 1H); 3.79-3.70 (m, 2H); 3.77 (s, 3H); 3.57 (d, 1H); 3.55 (s, 3H); 3.47 (d, 1H); 3.29 (d, 1H); 2.97 (d, 2H); 2.73-2.68 (m, 2H); 2.54 (d, 1H); 2.26 (s, 3H); 2.24-2.12 (m, 1H); 2.08 (s, 3H); 2.05 (s, 3H); 1.51 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 167.0, 151.5, 149.8, 147.4, 146.2, 142.1, 141.9, 139.8, 139.7, 132.8, 132.6, 131.1, 129.2, 126.7, 123.3, 122.7, 121.5, 117.9, 114.4, 112.4, 111.3, 102.8, 84.1, 71.5, 62.0, 60.6, 60.3, 59.6, 55.4, 54.5, 42.7, 42.2, 41.8, 39.0, 29.0, 27.7, 24.4, 15.8, 9.6.

ESI-MS m/z: Calcd. for C₄₇H₄₆F₆N₄O₁₃S: 1020.2 Found (M+H⁺): 1021.3.

EXAMPLE 95

The reaction is performed with 6 equiv. of anhydride and 9 equiv. of base (Method A). Traces of compound 110 is also obtained when the acylation reaction is performed with pyridine as base and compound 108 is the main product.

110. ¹H-NMR (300 MHz, CDCl₃): δ 6.92 (s, 1H); 6.69 (s, 1H); 6.58 (s, 1H); 6.03 (d, 1H); 5.96 (d, 1H); 4.99 (d, 1H); 4.64 (s, 1H); 4.27 (s, 2H); 4.13 (s, 1H); 4.12 (dd, 1H); 3.97 (d, 1H); 3.80 (s, 3H); 3.59 (s, 3H); 3.53 (d, 1H); 3.43-3.41 (m, 1H); 3.15-3.05 (m, 1H); 2.97-2.95 (m, 2H); 2.80-2.74 (m, 1H); 2.70-2.60 (m, 1H); 2.50-2.45 (m, 1H); 2.37-2.18 (m, 1H); 2.31 (s, 3H); 2.17 (s, 3H); 2.09 (s, 3H); 1.53 (s, 9H); 1.51 (s, 9H); 1.48 (s, 9H).

ESI-MS m/z: Calcd. for C₅₃H₆₄N₄O₁₅S: 1028.4 Found (M+H⁺): 1029.3.

EXAMPLE 96

Method B: To a solution of 1 equiv. of compound 106 in CH₂Cl₂ (0.032M) under Argon at room temperature were added 2 equiv. of base and 2 equiv. of the acid chloride. The reaction was followed by TLC and quenched with NaHCO₃, extracted with CH₂Cl₂ and the organic layers dried with Na₂SO₄. Flash chromatography gives pure compounds.

111 was obtained using Method B. ¹H-NMR (300 MHz, CDCl₃): δ 6.68 (s, 1H); 6.58 (s, 1H); 6.56 (s, 1H); 6.00 (dd, 2H); 5.67 (s, 1H); 5.00 (d, 1H); 4.58 (s, 1H); 4.36 (s, 1H); 4.27 (dd, 1H); 4.19 (d 1H); 4.12 (dd, 1H); 3.77 (s, 3H); 3.59 (s, 3H); 3.51 (d, 1H); 3.43-3.40 (m, 1H); 3.17-3.08 (m, 1H); 2.92 (d, 2H); 2.86-2.78 (m, 1H); 2.72-2.60 (m, 1H); 2.52-2.44 (m, 1H); 2.50 (t, 2H); 2.34-2.04 (m, 2H); 2.32 (s, 3H); 2.18 (s, 3H); 2.01 (s, 3H); 1.82-1.67 (m, 2H); 1.50 (s, 9H); 1.00 (t, 3H).

ESI-MS m/z: Calcd. for C₄₇H₅₄N₄O₁₂S: 898.3 Found (M+H⁺): 899.3.

EXAMPLE 97

Compound 111 is also isolated as minor compound in these reaction conditions (10 equiv. of butyryl chloride and 10 equiv. of TEA).

112 was obtained using Method B. ¹H-NMR (300 MHz, CDCl₃): δ 6.93 (s, 1H); 6.69 (s, 1H); 6.54 (s, 1H); 6.05 (s, 1H); 5.97 (s, 1H); 4.99 (d, 1H); 4.54 (s, 1H); 4.32 (s, 1H); 4.16 (d, 1H); 4.07 (dd, 1H); 3.79 (d, 1H); 3.74 (s, 3H); 3.69-3.31 (m, 1H); 3.58 (s, 3H); 3.52 (d, 1H); 3.43 (s, 1H); 3.18-3.08 (m, 1H); 2.98 (d, 2H); 2.85-2.79 (m, 1H); 2.68-2.44 (m, 2H); 2.60 (t, 2H); 2.55 (t, 2H); 2.31 (s, 3H); 2.14 (s, 3H); 2.02 (s, 3H); 1.89-1.74 (m, 4H); 1.50 (s, 9H); 1.08 (t, 3H); 1.01 (t, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.1, 171.3, 151.8, 148.8, 148.2, 145.7, 143.9, 141.5, 140.3, 139.1, 132.4, 131.7, 130.9, 128.8, 127.4, 124.6, 122.4, 120.8, 119.9, 118.1, 114.0, 112.0, 105.0, 102.2, 83.7, 61.2, 60.3, 59.9, 59.6, 56.1, 55.4, 54.5, 42.6, 42.2, 41.8, 39.8, 36.3, 36.0, 29.9, 28.7, 27.8, 24.3, 18.9, 18.5, 16.0, 14.1, 14.0, 10.0.

ESI-MS m/z: Calcd. for C₅₁H₆₀N₄O₁₃S: 968.3 Found (M+H⁺): 969.3.

EXAMPLE 98

113 was obtained using Method B. ¹H-NMR (300 MHz, CDCl₃): δ 7.88 (d, 1H); 7.62-7.58 (m, 2H); 7.47-7.44 (m, 3H); 6.70 (s, 1H); 6.59 (d, 1H); 6.58 (s, 1H); 6.54 (s, 1H); 6.03 (dd, 2H); 5.42 (s, 1H); 5.01 (d, 1H); 4.58 (s, 1H); 4.36 (s, 1H); 4.26 (dd, 1H); 4.19 (d 1H); 4.12 (dd, 1H); 3.61 (s, 3H); 3.55 (d, 1H); 3.46 (s, 3H); 3.43-3.40 (m, 1H); 3.16-3.08 (m, 1H); 2.92 (d, 2H); 2.86-2.78 (m, 1H); 2.72-2.60 (m, 1H); 2.52-2.44 (m, 1H); 2.34-2.04 (m, 2H); 2.47 (s, 3H); 2.17 (s, 3H); 2.08 (s, 3H); 1.50 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.2, 151.8, 148.8, 147.9, 145.6, 143.2, 141.3, 141.6, 140.4, 139.1, 134.4, 132.6, 131.0, 129.6, 129.3, 129.1, 128.8, 128.4, 122.4, 121.5, 120.7, 118.3, 118.1, 116.8, 114.3, 112.1, 102.1, 83.6, 65.2, 61.4, 60.2, 59.9, 59.5, 55.4, 54.8, 54.7, 42.4, 42.3, 41.8, 39.8, 29.9, 28.7, 27.8, 24.3, 15.9, 10.0.

ESI-MS m/z: Calcd. for C₅₂H₅₄N₄O₁₂S: 958.3 Found: (M+H⁺): 959.3.

EXAMPLE 99

114 was obtained using Method B. ¹H-NMR (300 MHz, CDCl₃): δ 7.85 (d, 2H); 7.55-7.21 (m, 10H); 6.93 (s, 1H); 6.73 (s, 1H); 6.70-6.50 (m, 2H); 6.56 (s, 1H); 6.09 (s, 1H); 5.99 (s, 1H); 5.03 (d, 1H); 4.53 (s, 1H); 4.39 (s, 1H); 4.21 (d, 1H); 4.11 (dd 1H); 3.91 (d, 1H); 3.61 (s, 3H); 3.45 (s, 3H); 3.20-3.11 (m, 1H); 2.99 (d, 2H); 2.74-2.65 (m, 1H); 2.53-2.47 (m, 1H); 2.28 (s, 3H); 2.17 (s, 3H); 2.11 (s, 3H); 1.52 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.1, 164.7, 164.3, 151.8, 148.8, 148.4, 147.5, 147.4, 145.9, 143.5, 141.5, 140.6, 139.1, 134.3, 133.9, 132.4, 131.7, 131.2, 131.0, 130.9, 129.2, 129.1, 128.9, 128.5, 128.3, 127.3, 124.5, 122.5, 121.3, 118.0, 116.6, 116.2, 114.3, 112.0, 102.2, 83.7, 65.4, 61.4, 60.2, 59.7, 59.2, 55.7, 55.3, 54.6, 42.7, 41.8, 39.9, 32.1, 31.8, 29.9, 29.6, 28.8, 27.8, 22.8, 16.0, 14.3, 10.1.

ESI-MS m/z: Calcd. for C₆₁H₆₀N₄O₁₃S: 1088.3 Found (M+H⁺): 1089.4.

EXAMPLE 100

115 was obtained using Method B. ¹H-NMR (300 MHz, CDCl₃): δ 6.69 (s, 1H); 6.58 (s, 2H); 6.04 (d, 1H); 5.99 (d, 1H); 5.96-5.85 (m, 1H); 5.71 (s, 1H); 5.38 (dd, 1H); 5.27 (dd, 1H); 5.00 (d, 1H); 4.67 (s, 1H); 4.64-4.61 (m, 2H); 4.30 (s, 1H); 4.28 (dd, 1H); 4.17 (d, 1H); 4.11 (dd, 1H); 3.77 (s, 3H); 3.58 (s, 3H); 3.50 (d, 1H); 3.41 (s, 1H); 3.16-3.08 (m, 1H); 2.93 (d, 2H); 2.81-2.74 (m, 1H); 2.69-2.59 (m, 1H); 2.51-2.45 (m, 1H); 2.39 (d, 1H); 2.31 (s, 3H); 2.21-2.16 (m, 1H); 2.19 (s, 3H); 2.09 (s, 3H); 1.50 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.3, 15.5, 151.8, 148.7, 148.1, 145.6, 143.2, 141.4, 140.5, 139.1, 132.7, 131.4, 130.9, 129.5, 128.8, 122.5, 121.5, 120.7, 119.1, 118.3, 118.2, 114.2, 113.5, 112.0, 102.2, 83.7, 69.4, 64.9, 61.3, 60.5, 60.2, 59.8, 55.4, 54.9, 54.8, 42.6, 41.8, 41.7, 39.7, 29.9, 28.8, 27.8, 24.3, 16.0, 9.5.

ESI-MS m/z: Calcd. for C₄₇H₅₂N₄O₁₃S: 912.3 Found (M+H⁺): 913.3.

EXAMPLE 101

116 was obtained using Method B. ¹H-NMR (300 MHz, CDCl₃): δ 6.69 (s, 1H); 6.58 (s, 1H); 6.56 (s, 1H); 6.05 (d, 1H); 5.98 (d, 1H); 5.74 (s, 1H); 5.00 (d, 1H); 4.52 (s, 1H); 4.32 (s, 1H); 4.27 (d, 1H); 4.17 (d, 1H); 4.09 (dd, 1H); 3.84 (ddd, 2H); 3.79 (s, 3H); 3.58 (s, 3H); 3.50 (d, 1H); 3.41 (s, 1H); 3.12-3.02 (m, 1H); 3.04 (t, 2H); 2.93 (d, 2H); 2.81-2.75 (m, 1H); 2.69-2.58 (m, 1H); 2.50-2.44 (m, 1H); 2.31 (s, 3H); 2.18 (s, 3H); 2.04 (s, 3H); 1.50 (s, 9H).

ESI-MS m/z: Calcd. for C₄₆H₅₁ClN₄O₁₂S: 918.3 Found (M+H⁺): 919.7.

EXAMPLE 102

117 was obtained using Method B. ¹H-NMR (300 MHz, CDCl₃): δ 6.70 (s, 1H); 6.58 (s, 1H); 6.54 (s, 1H); 6.11 (d, 1H); 6.04 (d, 1H); 5.67 (s, 1H); 5.02 (d, 1H); 4.46 (s, 1H); 4.33 (s, 2H); 4.29 (d, 1H); 4.20 (s, 1H); 4.11 (dd, 1H); 3.73 (s, 3H); 3.58 (s, 3H); 3.51 (d, 1H); 3.44 (s, 1H); 3.21-3.11 (m, 1H); 3.05-2.93 (m, 2H); 2.84-2.78 (m, 1H); 2.68-2.60 (m, 1H); 2.52-2.47 (m, 1H); 2.35 (s, 3H); 2.20 (s, 2H); 2.14 (s, 3H); 2.04 (s, 3H); 1.50 (s, 9H).

ESI-MS m/z: Calcd. for C₄₇H₄₇F₇N₄O₁₂S: 1024.3 Found (M+H⁺): 1025.2.

EXAMPLE 103

118 was obtained using Method B ¹H-NMR (300 MHz, CDCl₃): δ 6.98 (dd, 1H); 6.70 (s, 1H); 6.59 (s, 1H); 6.58 (s, 1H); 6.06 (d, 1H); 5.99 (d, 1H); 5.74 (s, 1H); 5.01 (d, 1H); 4.98 (dd, 1H); 4.65 (s, 1H); 4.60 (dd, 1H); 4.31 (s, 2H); 4.28 (d, 1H); 4.18 (s, 1H); 4.12 (dd, 1H); 3.75 (s, 3H); 3.58 (s, 3H); 3.50 (d, 1H); 3.41 (s, 1H); 3.18-3.10 (m, 1H); 2.93 (d, 2H); 2.81-2.74 (m, 1H); 2.68-2.58 (m, 1H); 2.51-2.46 (m, 1H); 2.38 (d, 1H); 2.31 (s, 3H); 2.20 (s, 3H); 2.10 (s, 3H); 1.50 (s, 9H).

ESI-MS m/z: Calcd. for C₄₆H₅₀N₄O₁₃S: 898.3 Found (M+H⁺): 899.3.

EXAMPLE 104

Method C: To a solution of 1 equiv. of compound 106 in CH₂Cl₂ (0.032M) under Argon were added 2 equiv. of acid, 2 equiv. of DMAP and 2 equiv. of EDC.HCl. The reaction was stirred at room temperature for 2 h. After this time was diluted with CH₂Cl₂, washed with brine and the organic layer dried with Na₂SO₄. Flash chromatography gives pure compounds.

119 was obtained using Method C. ¹H-NMR (300 MHz, CDCl₃): δ 6.68 (s, 1H); 6.58 (s, 1H); 6.56 (s, 1H); 6.00 (dd, 2H); 5.66 (s, 1H); 4.99 (d, 1H); 4.53 (s, 1H); 4.31 (s, 1H); 4.26 (dd, 1H); 4.16 (d, 1H); 4.09 (dd, 1H); 3.77 (s, 3H); 3.57 (s, 3H); 3.51 (d, 1H); 3.42-3.40 (m, 1H); 3.16-3.05 (m, 1H); 2.93 (d, 2H); 2.82-2.74 (m, 1H); 2.69-2.58 (m, 1H); 2.51-2.44 (m, 1H); 2.53 (t, 2H); 2.34-2.14 (m, 2H); 2.31(s, 3H); 2.18 (s, 3H); 2.01 (s, 3H); 1.75-1.70 (m, 2H); 1.50 (s, 9H); 1.35-1.25 (m, 11H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 170.8, 151.5, 148.5, 147.7, 145.3, 143.0, 141.4, 141.3, 140.0, 138.9, 132.4, 130.8, 129.2, 128.6, 122.1, 121.0, 120.6, 118.2, 118.0, 113.9, 111.9, 101.9, 83.3, 64.8, 61.0, 60.2, 60.1, 59.7, 59.6, 55.2, 54.7, 54.6, 42.3, 41.8, 41.5, 39.6, 33.9, 31.6, 29.6, 29.3, 28.9, 28.6, 27.5, 24.8, 24.2, 22.5, 15.7, 14.0, 9.7.

ESI-MS m/z: Calcd. for C₅₁H₆₂N₄O₁₂S: 954.4 Found (M+H⁺): 955.5.

EXAMPLE 105

120 is obtained with 10 equiv. of each reagent (Method C).

¹H-NMR (300 MHz, CDCl₃): δ 6.93 (s, 1H); 6.69 (s, 1H); 6.54 (s, 1H); 6.00 (dd, 2H); 4.99 (d, 1H); 4.44 (s, 1H); 4.31 (s, 1H); 4.16 (d, 1H); 4.09 (dd, 1H); 3.86 (d, 1H); 3.73 (s, 3H); 3.57 (s, 3H); 3.50 (d, 1H); 3.44-3.42 (m, 1H); 3.16-3.05 (m, 1H); 2.97 (d, 2H); 2.84-2.79 (m, 1H); 2.64-2.44 (m, 6H); 2.35-2.15 (m, 2H); 2.31 (s, 3H); 2.14 (s, 3H); 2.02 (s, 3H); 1.94-1.58 (m, 8H); 1.50 (s, 9H); 1.38-1.18 (m, 18H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.2, 171.4 170.8, 151.8, 148.8, 148.2, 145.7, 143.9, 141.5, 140.4, 139.1, 132.5, 131.6, 130.8, 128.8, 127.4, 124.7, 122.4, 120.9 118.0, 114.1, 112.1, 102.2, 83.6, 65.1, 61.3, 60.3, 60.2, 59.9, 59.5, 56.1, 55.4, 54.6, 42.6, 42.2, 41.8, 39.8, 34.4, 34.1, 31.8, 29.6, 29.5, 29.2, 29.1, 29.0, 28.8, 27.8, 25.4, 24.9, 22.8, 16.0, 14.2, 9.9.

ESI-MS m/z: Calcd. for C₅₉H₇₆N₄O₁₃S: 1080.5 Found (M+H⁺): 1081.3.

EXAMPLE 106

It was used 1 equiv. of palmitic acid (Method C).

121: ¹H-NMR (300 MHz, CDCl₃): δ 6.68 (s, 1H); 6.58 (s, 1H); 6.56 (s, 1H); 6.00 (dd, 2H); 5.66 (s, 1H); 4.99 (d, 1H); 4.53 (s, 1H); 4.31 (s, 1H); 4.26 (dd, 1H); 4.16 (d, 1H); 4.09 (dd, 1H); 3.77 (s, 3H); 3.58 (s, 3H); 3.51 (d, 1H); 3.42-3.40 (m, 1H); 3.16-3.08 (m, 1H); 2.93 (d, 2H); 2.84-2.76 (m, 1H); 2.69-2.44 (m, 2H); 2.53 (t, 2H); 2.35-2.15 (m, 2H); 2.31 (s, 3H); 2.18 (s, 3H); 2.01 (s, 3H); 1.74-1.69 (m, 2H); 1.50 (s, 9H); 1.38-1.10 (m, 27H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 171.8, 148.4, 148.0, 145.5, 143.2, 141.6, 140.2, 139.1, 137.4, 132.6, 131.0, 129.5, 128.8, 122.4, 121.2, 120.9, 118.3, 114.2, 112.1, 102.0, 65.1, 61.3, 60.5, 60.3, 59.9, 59.8, 55.4, 54.9, 54.8, 42.5, 42.0, 41.8, 39.8, 34.2, 32.1, 29.9, 29.7, 29.6, 29.5, 28.8, 27.8, 25.1, 24.4, 22.8, 16.0, 14.3, 9.9.

ESI-MS m/z: Calcd. for C₅₉H₇₈N₄O₁₂S: 1066.5 Found (M+H⁺): 1067.4.

122: ¹H-NMR (300 MHz, CDCl₃): δ 6.94 (s, 1H); 6.70 (s, 1H); 6.55 (s, 1H); 6.02 (dd, 2H); 5.00 (d, 1H); 4.46 (s, 1H); 4.33 (s, 1H); 4.18 (d, 1H); 4.09 (dd, 1H); 3.79 (d, 1H); 3.74 (s, 3H); 3.58 (s, 3H); 3.52 (d, 1H); 3.46-3.43 (m, 1H); 3.15-3.05 (m, 1H); 2.99-2.97 (m, 2H); 2.68-2.45 (m, 7H); 2.36-2.11 (m, 2H); 2.32 (s, 3H); 2.15 (s, 3H); 2.03 (s, 3H); 1.86-1.60 (m, 4H); 1.50 (s, 9H); 1.40-1.10 (m, 54H).

ESI-MS m/z: Calcd. for C₇₅H₁₀₈N₄O₁₃S: 1302.7 Found (M+H⁺): 1303.6.

EXAMPLE 107

Compound 124 is isolated impurified with DMAP.

123 was obtained using Method C: ¹H-NMR (300 MHz, CDCl₃): δ 7.74 (s, 1H); 6.96 (s, 1H); 6.69 (s, 1H); 6.54 (s, 2H); 6.04 (d, 1H); 5.96 (d, 1H); 5.09(s, 1H); 5.00 (d, 1H); 4.51-4.48 (m, 2H); 4.34 (s, 2H); 4.30 (d, 1H); 4.19 (d, 1H); 4.06 (dd, 1H); 3.75 (s, 3H); 3.57 (s, 3H); 3.52 (d, 1H); 3.41 (s, 1H); 3.19-3.08 (m, 2H); 2.92-2.80 (m, 3H); 2.75-2.44 (m, 5H); 2.29 (s, 3H); 2.17 (s, 3H); 2.01 (s, 3H); 2.82-1.66 (m, 6H); 1.50 (s, 9H).

ESI-MS m/z: Calcd. for C₅₃H₆₂N₆O₁₃S₂: 1055.2 Found (M+H⁺): 1056.3.

124 was obtained using Method C: ESI-MS m/z: Calcd. for C₆₃H₇₆N₈O₁₅S₃: 1281.5 Found (M+H⁺): 1282.4.

EXAMPLE 108

125 was obtained using Method C ¹H-NMR (300 MHz, CDCl₃): δ 6.69 (s, 1H); 6.55 (s, 2H); 6.05 (d, 1H); 5.97 (d, 1H); 5.00 (d, 1H); 4.61 (t, 1H); 4.51 (s, 1H); 4.34 (s, 1H); 4.27 (d, 1H); 4.18 (d, 1H); 4.12-4.06 (m, 2H); 3.76 (s, 3H); 3.57 (s, 3H); 3.50 (d, 1H); 3.42 (s, 1H); 3.14-3.06 (m, 1H); 2.92 (d, 1H); 2.84-2.80 (m, 1H); 2.69-2.60 (m, 1H); 2.50-2.45 (m, 1H); 2.30 (s, 3H); 2.17 (s, 3H); 2.02 (s, 3H); 1.61 (d, 3H); 1.50 (s, 9H); 1.43 (s, 9H).

ESI-MS m/z: Calcd. for C₅₁H₆₁N₅O₁₄S: 999.4 Found (M+H⁺): 1000.3.

EXAMPLE 109

Method E: To a solution of 1 equiv. of compound 106 in DMF (0.032M) under Argon at room temperature were added 2 equiv. of Cs₂CO₃ and 2 equiv. of the allyl bromide. The reaction was followed by TLC and quenched with NaHCO₃, extracted with CH₂Cl₂ and the organic layers dried with Na₂SO₄. Flash chromatography gives pure compounds.

126: was obtained using Method E ¹H-NMR (300 MHz, CDCl₃): δ 6.70 (s, 1H); 6.58 (s, 2H); 5.97 (d, 1H); 5.90 (d, 1H); 5.79 (s, 1H); 5.00 (d, 1H); 4.88 (s, 1H); 4.30-4.29 (m, 3H); 4.15-4.11 (m, 2H); 3.85-3.82 (m, 2H); 3.80 (s, 3H); 3.58 (s, 3H); 3.51 (d, 1H); 3.40 (s, 1H); 3.12-3.00 (m, 1H); 2.92 (d, 2H); 2.83-2.79 (m, 1H); 2.67-2.60 (m, 1H); 2.50-2.44 (m, 1H); 2.31 (s, 3H); 2.28-2.37 (m, 1H); 2.20 (s, 3H); 2.18 (s, 3H); 1.50 (s, 9H).

ESI-MS m/z: Calcd. for C₄₄H₅₀N₄O₁₁S: 842.3 Found (M+H⁺): 843.4.

127 was obtained using Method E: ¹H-NMR (300 MHz, CDCl₃): δ 6.75 (s, 1H); 6.71 (s, 1H); 6.58 (s, 1H); 5.98 (s, 1H); 5.91 (s, 1H); 5.01 (d, 1H); 4.81 (s, 1H); 4.29 (s, 1H); 4.26 (dd, 1H); 4.15 (s, 1H); 4.13 (dd, 1H); 3.96 (s, 3H); 3.85-3.74 (m, 1H); 3.83 (s, 3H); 3.74 (s, 3H); 3.58 (s, 3H); 3.50 (d, 1H); 3.41 (s, 1H); 3.10-3.04 (m, 1H); 2.93 (d, 2H); 2.85-2.80 (m, 1H); 2.70-2.59 (m, 1H); 2.51-2.44 (m, 1H); 2.31-2.20 (m, 1H); 2.28 (s, 3H); 2.24 (s, 3H); 2.18 (s, 3H); 1.51 (s, 9H).

ESI-MS m/z: Calcd. for C₄₅H₅₂N₄O₁₁S: 856.3 Found (M+H⁺): 857.3.

EXAMPLE 110

Compound 106 (15%) is recovered after chromatographic purification.

128: was obtained using Method E. ^(0.1)H-NMR (300 MHz, CDCl₃): δ 6.70 (s, 1H); 6.59 (s, 1H); 6.58 (s, 1H); 5.97 (s, 1H); 5.90 (s, 1H); 5.75 (s, 1H); 5.01 (d, 1H); 4.91 (s, 1H); 4.29 (s, 2H); 4.16 (s, 1H); 4.14 (dd, 1H); 3.82 (q, 2H); 3.80 (s, 3H); 3.58 (s, 3H); 3.50 (d, 1H); 3.41 (s, 1H); 3.11-3.03 (m, 1H); 2.92 (d, 2H); 2.84-2.80 (m, 1H); 2.70-2.60 (m, 1H); 2.50-2.45 (m, 1H); 2.31 (s, 3H); 2.23 (s, 2H); 2.20 (s, 3H); 2.17 (s, 3H); 1.50 (s, 9H); 1.39 (t, 3H).

ESI-MS m/z: Calcd. for C₄₅H₅₂N₄O₁₁S: 856.3 Found (M+H⁺): 857.3.

129 was obtained using Method E: ¹H-NMR (300 MHz, CDCl₃): δ 6.75 (s, 1H); 6.70 (s, 1H); 6.58 (s, 1H); 5.97 (d, 1H); 5.91 (d, 1H); 5.00 (d, 1H); 4.87 (s, 1H); 4.29-4.26 (m, 2H); 4.1-4.13 (m, 2H); 3.89-3.81 (m, 4H); 3.85 (s, 3H); 3.58 (s, 3H); 3.50 (d, 1H); 3.42 (s, 1H); 3.11-3.04 (m, 1H); 2.94 (d, 2H); 2.85-2.80 (m, 1H); 2.70-2.60 (m, 1H); 2.52-2.44 (m, 1H); 2.27 (s, 3H); 2.22 (s, 2H); 2.20 (s, 3H); 2.17 (s, 3H); 1.51 (s, 9H); 1.41 (t, 3H); 1.40 (t, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 151.8, 151.0, 149.6, 149.0, 148.7, 145.8, 139.0, 138.7, 132.6, 131.4, 130.5, 129.0, 124.7, 124.3, 122.5, 122.0, 118.3, 114.0, 113.2, 111.9, 101.7, 83.7, 69.2, 68.2, 65.6, 61.7, 60.6, 60.3, 59.7, 59.6, 55.3, 54.9, 42.9, 42.1, 41.9, 39.8, 29.9, 28.9, 27.8, 24.5, 16.4, 16.0, 15.6, 9.8.

ESI-MS m/z: Calcd. for C₄₇H₅₆N₄O₁₁S: 884.3 Found (M+H⁺): 885.5.

EXAMPLE 111

Compound 106 (33%) is recovered after chromatographic purification.

130 was obtained using Method E: ¹H-NMR (300 MHz, CDCl₃): δ 6.70 (s, 1H); 6.58 (s, 2H); 5.96 (s, 1H); 5.90 (s, 1H); 5.68 (s, 1H); 5.00 (d, 1H); 4.90 (s, 1H); 4.29 (s, 2H); 4.15 (s, 1H); 4.13 (dd, 1H); 3.85-3.78 (m, 2H); 3.79 (s, 3H); 3.58 (s, 3H); 3.50 (d, 1H); 3.40 (s, 1H); 3.12-3.04 (m, 1H); 2.92 (d, 2H); 2.86-2.80 (m, 1H); 2.71-2.60 (m, 1H); 2.50-2.43 (m, 1H); 2.30 (s, 3H); 2.23 (s, 2H); 2.19 (s, 3H); 2.16 (s, 3H); 1.83-1.76 (m, 2H); 1.50 (s, 9H); 1.06 (t, 3H).

ESI-MS m/z: Calcd. for C₄₆H₅₄N₄O₁₁S: 871.3 Found (M+H⁺): 872.5.

131 was obtained using Method E: ¹H-NMR (300 MHz, CDCl₃): δ 6.75 (s, 1H); 6.70 (s, 1H); 6.58 (s, 1H); 5.97 (d, 1H); 5.90 (d, 1H); 5.00 (d, 1H); 4.88 (s, 1H); 4.28-4.11 (m, 4H); 3.85 (s, 3H); 3.82-3.64 (m, 4H); 3.58 (s, 3H); 3.51 (d, 1H); 3.41 (s, 1H); 3.12-3.05 (m, 1H); 2.94 (d, 2H); 2.86-2.80 (m, 1H); 2.74-2.62 (m, 1H); 2.51-2.46 (m, 1H); 2.27 (s, 3H); 2.22 (s, 2H); 2.20 (s, 3H); 2.16 (s, 3H); 1.81-1.75 (m, 4H); 1.50 (s, 9H); 1.07 (t, 3H); 1.02 (t, 3H). ¹³C-NMR (75 MHz, CDCl₃): δ 170.9, 150.6, 150.0, 148.3, 147.8, 147.4, 144.6, 137.8, 137.4, 131.4, 130.1, 129.3, 127.8, 123.4, 123.1, 121.3, 120.7, 117.1, 112.7, 112.0, 110.7, 100.4, 82.4, 73.6, 73.3, 64.4, 60.4, 59.5, 59.1, 58.6, 58.5, 54.1, 54.0, 53.6, 41.8, 40.8, 40.7, 38.6, 28.6, 27.7, 26.5, 23.3, 22.9, 22.4, 14.7, 9.9, 9.4, 8.5.

ESI-MS m/z: Calcd. for C₄₉H₆₀N₄O₁₁S: 912.4 Found (M+H⁺): 913.5.

EXAMPLE 112

With 1 equiv. of allyl bromide and 1 equiv. of cesium carbonate the reaction is complete and other fraction is isolated after chromatographic purification which is a mixture of compound 131 and compound 132 (Method E).

132: ¹H-NMR (300 MHz, CDCl₃): δ 6.70 (s, 1H); 6.58 (s, 2H); 6.15-6.02 (m, 1H); 5.98 (d, 1H); 5.91 (d, 1H); 5.69 (s, 1H); 5.43 (dd, 1H); 5.26 (d, 1H); 5.01 (d, 1H); 4.91 (s, 1H); 4.48 (dd, 1H); 4.29-4.28 (m, 2H); 4.23-4.12 (m, 3H); 3.80 (s, 3H); 3.58 (s, 3H); 3.50 (d, 1H); 3.41 (s, 1H); 3.12-3.03 (m, 1H); 2.95-2.91 (m, 2H); 2.88-2.80 (m, 1H); 2.70-2.60 (m, 1H); 2.50-2.45 (m, 1H); 2.31 (s, 3H); 2.24 (s, 2H); 2.20 (s, 3H); 2.18 (s, 3H); 1.51 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.3, 168.5, 152.0, 149.7, 148.9, 148.2, 146.0, 143.5, 139.3, 139.0, 134.0, 132.8, 131.3, 129.7, 129.3, 129.2, 122.7, 122.2, 121.0, 118.5, 118.4, 117.9, 114.2, 113.4, 112.1, 101.9, 83.9, 74.5, 65.8, 61.8, 60.8, 60.6, 60.0, 55.5, 55.1, 55.1, 43.1, 42.3, 42.0, 40.1, 30.1, 29.1, 28.0, 24.6, 16.2, 14.5, 10.1.

ESI-MS m/z: Calcd. for C₄₆H₅₂N₄O₁₁S: 868.3 Found (M+H⁺): 869.3.

Compound 133: ¹H-NMR (300 MHz, CDCl₃): δ 6.77 (s, 1H); 6.70 (s, 1H); 6.58 (s, 1H); 6.14-6.01 (m, 2H); 5.97 (s, 1H); 5.91 (s, 1H) 5.43 (dd, 1H); 5.37 (dd, 1H); 5.23 (dd, 1H); 5.19 (dd, 1H); 5.00 (d, 1H); 4.89 (s, 1H); 4.78 (dd, 1H); 4.71-4.36 (m, 2H); 4.28-4.12 (m, 4H); 3.84 (s, 3H); 3.58 (s, 3H); 3.50 (d, 1H); 3.41 (s, 1H); 3.12-3.03 (m, 1H); 2.93 (d, 2H); 2.86-2.80 (m, 1H); 2.72-2.60 (m, 1H); 2.51-2.46 (m, 1H); 2.28 (s, 3H); 2.23 (s, 2H); 2.18 (s, 3H); 2.17 (s, 3H); 1.50 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.1, 151.8, 150.8, 149.3, 149.0, 148.7, 145.8, 139.1, 138.8, 134.7, 133.6, 132.5, 131.4, 130.5, 129.0, 124.7, 124.5, 122.5, 122.0, 118.3, 118.0, 117.2, 113.9, 113.2, 111.8, 101.7, 83.7, 74.2, 73.3, 65.6, 61.6, 60.5, 60.3, 59.8, 59.7, 55.3, 54.8, 43.0, 42.0, 41.9, 39.8, 38.9, 27.8, 24.5, 16.0, 9.9.

ESI-MS m/z: Calcd. for C₄₉H₅₆N₄O₁₁S: 909.1 Found (M+H⁺): 910.3.

EXAMPLE 113

134 was obtained using Method E: ¹H-NMR (300 MHz, CDCl₃): δ 7.52-7.50 (m, 2H); 7.43-7.37 (m, 3H); 6.70 (s, 1H); 6.61 (s, 1H); 6.57 (s, 1H); 5.97 (dd, 2H); 5.56 (s, 1H); 5.01 (d, 1H); 4.99 (d, 1H); 4.87 (s, 1H); 4.74 (d, 1H); 4.30 (s, 1H); 4.20-4.14 (m, 3H); 3.76 (s, 3H); 3.60 (s, 3H); 3.41 (d, 2H); 3.13-3.02 (m, 1H); 2.90-2.88 (m, 2H); 2.88-2.78 (m, 1H); 2.64-2.58 (m, 1H); 2.51-2.44 (m, 1H); 2.34-2.10 (m, 2H); 2.30 (s, 3H); 2.24 (s, 3H); 2.17 (s, 3H); 1.50 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.1, 149.0, 148.7, 148.0, 145.9, 139.0, 137.4, 132.6, 131.1, 129.5, 129.1, 128.7, 128.6, 128.3, 128.2, 122.5, 120.8, 118.3, 118.2, 114.1, 113.4, 112.0, 101.8, 83.7, 74.8, 65.6, 61.8, 60.6, 60.4, 59.7, 55.4, 54.8, 43.0, 42.2, 41.8, 39.9, 29.9, 29.0, 27.8, 24.4, 16.0, 9.9.

ESI-MS m/z: Calcd. for C₅₀H₅₄N₄O₁₁S: 918.3 Found (M+H⁺): 919.3.

135 was obtained using Method E: ¹H-NMR (300 MHz, CDCl₃): δ 7.47-7.43 (m, 2H); 7.32-7.20 (m, 8H); 6.79 (s, 1H); 6.71 (s, 1H); 6.62 (s, 1H); 5.96 (dd, 2H); 5.24 (d, 1H); 5.03-4.93 (m, 4H); 4.68 (d, 1H); 4.28 (s, 1H); 4.18-4.08 (m, 3H); 3.87 (s, 3H); 3.60 (s, 3H); 3.43 (d, 1H); 3.35-3.32 (m, 1H); 3.15-3.08 (m, 1H); 2.92-2.91 (m, 2H); 2.88-2.80 (m, 1H); 2.72-2.60 (m, 1H); 2.54-2.46 (m, 1H); 2.32 (s, 3H); 2.23 (s, 3H); 2.22 (d, 1H); 2.05 (d, 1H); 1.84 (s, 3H); 1.51 (s, 9H).

ESI-MS m/z: Calcd. for C₅₇H₆₀N₄O₁₁S: 1008.4 Found (M+H⁺): 1009.3.

EXAMPLE 114

Method F: To a solution of 1 equiv. of starting material in CH₂Cl₂/H₂O/TFA 2:1:3.3 (0.013M) was stirred at room temperature for 15 min. The reaction was followed by TLC and neutralised with NaHCO₃, extracted with CH₂Cl₂ and the organic layers dried over Na₂SO₄. Flash chromatography gives pure compounds.

136 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.61 (s, 1H); 6.49 (s, 1H); 6.39 (s, 1H); 5.92 (dd, 2H); 5.69 (s, 1H); 4.90 (d, 1H); 4.48 (s, 1H); 4.34 (s, 1H); 4.31 (dd, 1H); 4.16 (d, 1H); 4.03 (dd, 1H); 3.79 (s, 3H); 3.63-3-59 (m, 1H); 3.60 (s, 3H); 3.44-3.40 (m, 1H); 3.16-3.08 (m, 1H); 2.94 (d, 2H); 2.82-2.73 (m, 1H); 2.69-2.54 (m, 1H); 2.51-2.46 (m, 1H); 2.41-2.24 (m, 2H); 2.39 (s, 3H); 2.19 (s, 3H); 2.16 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 148.2, 146.4, 144.5, 136.3, 130.8, 129.6, 125.9, 120.9, 118.3, 114.5, 113.4, 109.7, 101.4, 64.2, 61.1, 60.7, 60.0, 59.3, 55.4, 54.9, 54.8, 43.3, 41.7, 41.5, 39.8, 29.9, 29.5, 28.9, 24.4, 16.1, 14.3, 8.9.

ESI-MS m/z: Calcd. for C₃₈H₄₀N₄O₉S: 728.2 Found (M+H⁺): 729.3.

EXAMPLE 115

137 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 7.87 (d, 1H); 7.60-7.57 (m, 2H); 7.46-7.44 (m, 3H); 6.58 (d, 1H); 6.54 (s, 1H); 6.49 (s, 1H); 6.45 (s, 1H); 6.03 (dd, 2H); 5.42 (s, 1H); 5.02 (d, 1H); 4.60 (s, 1H); 4.36 (s, 1H); 4.26 (dd, 1H); 4.19 (d, 1H); 4.13 (dd, 1H); 3.64 (s, 3H); 3.55 (d, 1H); 3.44 (s, 3H); 3.44-3.40 (m, 1H); 3.16-3.08 (m, 1H); 2.92 (d, 2H); 2.84-2.78 (m, 1H); 2.69-2.58 (m, 1H); 2.49-2.42 (m, 1H); 2.38-2.29 (m, 2H); 2.24 (s, 3H); 2.17 (s, 3H); 2.09 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.2, 147.9, 146.7, 145.6, 144.7, 144.5, 143.2, 141.6, 134.4, 131.0, 129.5, 129.3, 128.4, 125.9, 121.7, 120.8, 118.3, 118.1, 116.9, 114.4, 114.2, 110.0, 102.0, 65.0, 61.4, 60.2, 60.1, 59.9, 59.5, 55.3, 54.9, 54.8, 42.5, 42.3, 41.8, 39.9, 32.1, 31.7, 30.6, 29.9, 29.0, 24.3, 22.8, 15.9, 14.3, 10.0.

ESI-MS m/z: Calcd. for C₄₇H₄₆N₄O₁₀: 858.2 Found (M+H⁺): 859.3.

EXAMPLE 116

138 was obtained using Method F ¹H-NMR (300 MHz, CDCl₃): δ 7.87 (d, 1H); 7.82 (d, 1H); 7.56-7.53 (m, 4H); 7.46-7.31 (m, 6H); 6.93 (s, 1H); 6.64 (d, 1H); 6.52 (d, 1H); 6.51 (s, 1H); 6.43 (s, 1H); 6.10 (s, 1H); 6.00 (s, 1H); 5.43 (s, 1H); 5.04 (d, 1H); 4.55 (s, 1H); 4.40 (s, 1H); 4.23 (d, 1H); 4.13 (dd, 1H); 3.92 (d, 1H); 3.65 (s, 3H); 3.59 (d, 1H); 3.51-3.46 (m, 1H); 3.44 (s, 3H); 3.19-3.11 (m, 1H); 3.00 (d, 2H); 2.93-2.86 (m, 1H); 2.74-2.63 (m, 1H); 2.50-2.45 (m, 1H); 2.36-2.24 (m, 2H); 2.28 (s, 3H); 2.17 (s, 3H); 2.13 (s, 3H).

ESI-MS m/z: Calcd. for C₅₆H₅₂N₄O₁₁S: 989.1 Found (M+H⁺): 990.2.

EXAMPLE 117

139 was obtained using Method F ¹H-NMR (300 MHz, CDCl₃): δ 6.58 (s, 1H); 6.47 (s, 1H); 6.43 (s, 1H); 6.04 (d, 1H); 5.97 (d, 1H); 5.67 (s, 1H); 5.41 (s, 1H); 5.01 (d, 1H); 4.55 (s, 1H); 4.32 (s, 1H); 4.26 (d, 1H); 4.18 (d, 1H); 4.11 (dd, 1H); 3.78 (s, 3H); 3.61 (s, 3H); 3.51 (d, 1H); 3.41 (s, 1H); 3.15-3.08 (m, 1H); 2.93 (d, 2H); 2.82-2.76 (m, 1H); 2.61-2.42 (m, 2H); 2.53 (t, 2H); 2.31 (s, 3H); 2.18 (s, 3H); 2.02 (s, 3H); 1.79-1.72 (m, 2H); 1.02 (t, 3H).

ESI-MS m/z: Calcd. for C₄₂H₄₆N₄O₁₀S: 798.3 Found (M+H⁺): 799.3.

EXAMPLE 118

140 was obtained using Method F ¹H-NMR (300 MHz, CDCl₃): δ 6.94 (s, 1H); 6.48 (s, 1H); 6.41 (s, 1H); 6.06 (d, 1H); 5.98 (d, 1H); 5.42 (s, 1H); 5.01 (d, 1H); 4.47 (s, 1H); 4.32 (s, 1H); 4.18 (d, 1H); 4.11 (dd, 1H); 3.81-3.66 (m, 2H); 3.74 (s, 3H); 3.61 (s, 3H); 3.51 (d, 1H); 3.44 (s, 1H); 3.16-3.06 (m, 1H); 2.98 (d, 2H); 2.83-2.79 (m, 1H); 2.64-2.48 (m, 2H); 2.60 (t, 2H); 2.55 (t, 2H); 2.32 (s, 3H); 2.15 (s, 3H); 2.03 (s, 3H); 1.93-1.73 (m, 4H); 1.09 (t, 3H); 1.01 (t, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 171.4, 170.0, 147.0, 144.4, 143.5, 143.2, 142.6, 140.3, 139.1, 130.4, 129.6, 128.1, 126.2, 124.4, 123.4, 119.8, 116.8, 113.0, 112.9, 108.7, 100.7, 63.7, 60.1, 59.0, 58.9, 58.7, 58.3, 54.9, 54.0, 53.4, 41.4, 40.9, 40.6, 38.7, 35.0, 34.8, 28.6, 27.7, 23.0, 17.6, 17.2, 14.8, 12.9, 12.8, 8.7.

ESI-MS m/z: Calcd. for C₄₆H₅₂N₄O₁₁S: 868.3 Found (M+H⁺): 869.3.

EXAMPLE 119

141 was obtained using Method F ¹H-NMR (300 MHz, CDCl₃): δ 6.58 (s, 1H); 6.47 (s, 1H); 6.45 (s, 1H); 6.05 (d, 1H); 5.98 (d, 1H); 5.72 (s, 1H); 5.37 (dd, 1H); 5.26 (dd, 1H); 5.01 (d, 1H); 4.67 (s, 1H); 4.62 (d, 1H); 4.31 (s, 1H); 4.26 (d, 1H); 4.18 (d, 1H); 4.13 (dd, 1H); 3.77 (s, 3H); 3.61 (s, 3H); 3.50 (d, 1H); 3.41 (s, 1H); 3.16-3.08 (m, 1H); 2.93 (d, 2H); 2.80-2.74 (m, 1H); 2.68-2.56 (m, 1H); 2.48-2.36 (m, 2H); 2.31 (s, 3H); 2.19 (s, 3H); 2.18-2.14 (m, 2H); 2.09 (s, 3H).

ESI-MS m/z: Calcd. for C₄₂H₄₄N₄O₁₁S: 812.3 Found (M+H⁺): 813.3.

EXAMPLE 120

¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 1H); 6.47 (s, 1H); 6.43 (s, 1H); 6.06 (d, 1H); 5.99 (d, 1H); 5.75 (s, 1H); 5.41 (s, 1H); 5.01 (d, 1H); 4.53 (s, 1H); 4.33 (s, 1H); 4.27 (d, 1H); 4.18 (d, 1H); 4.11 (dd, 1H); 3.83 (ddd, 2H); 3.78 (s, 3H); 3.62 (s, 3H); 3.51 (d, 1H); 3.42 (s, 1H); 3.16-3.08 (m, 1H); 3.04 (t, 2H); 2.93 (d, 2H); 2.82-2.76 (m, 1H); 2.68-2.58 (m, 1H); 2.48.2.42 (m, 1H); 2.31 (s, 3H); 2.18 (s, 3H); 2.05 (s, 3H).

ESI-MS m/z: Calcd. for C₄₁H₄₃ClN₄O₁₀S: 818.2 Found (M+H⁺): 819.2.

EXAMPLE 121

143 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 1H); 6.49 (s, 1H); 6.45 (s, 1H); 6.10 (d, 1H); 6.03 (d, 1H); 5.68 (s, 1H); 5.47 (s, 1H); 5.04 (d, 1H); 4.57 (s, 1H); 4.34 (s, 1H); 4.29 (d, 1H); 4.21 (d, 1H); 4.14 (dd, 1H); 3.75 (s, 3H); 3.62 (s, 3H); 3.50 (d, 1H); 3.43 (s, 1H); 3.18-3.09 (m, 1H); 2.94 (d, 2H); 2.80-2.72 (m, 1H); 2.68-2.56 (m, 1H); 2.52-2.45 (m, 1H); 2.35-2.04 (m, 2H); 2.31 (s, 3H); 2.20 (s, 3H); 2.04 (s, 3H).

ESI-MS m/z: Calcd. for C₄₂H₃₉F₇N₄O₁₀S: 924.2 Found (M+H⁺): 925.2.

EXAMPLE 122

144 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 1H); 6.47 (s, 1H); 6.43 (s, 1H); 6.01 (dd, 2H); 5.68 (s, 1H); 5.01 (d, 1H); 4.56 (s, 1H); 4.32 (s, 1H); 4.27 (dd, 1H); 4.18 (d, 1H); 4.12 (dd, 1H); 3.78 (s, 3H); 3.62 (s, 3H); 3.51 (d, 1H); 3.43-3.40 (m, 1H); 3.18-3.06 (m, 1H); 2.93 (d, 2H); 2.82-2.76 (m, 1H); 2.63-2.44 (m, 2H); 2.53 (t, 2H); 2.36-2.15 (m, 2H); 2.32 (s, 3H); 2.19 (s, 3H); 2.02 (s, 3H); 1.75-1.70 (m, 2H); 1.40-1.21 (m, 11H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.5, 170.9, 147.7, 145.2, 144.5, 144.2, 143.0, 141.3, 140.0, 130.7, 129.2, 129.1, 127.1, 125.7, 121.1, 120.7, 118.1, 114.0, 113.2, 109.8, 101.7, 64.6, 61.1, 60.3, 60.0, 59.7, 59.6, 55.1, 54.7, 54.6, 42.2, 41.7, 41.5, 39.7, 34.0, 31.6, 29.6, 29.3, 28.9, 28.7, 24.8, 24.2, 22.5, 15.7, 14.0, 9.7.

ESI-MS m/z: Calcd. for C₄₆H₅₄N₄O₁₀S: 854.3 Found (M+H⁺): 855.3.

EXAMPLE 123

145 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.94 (s, 1H); 6.47 (s, 1H); 6.41 (s, 1H); 6.01 (dd, 2H); 5.01 (d, 1H); 4.47 (s, 1H); 4.32 (s, 1H); 4.18 (d, 1H); 4.11 (dd, 1H); 3.79 (d, 1H); 3.73 (s, 3H); 3.61 (s, 3H); 3.50 (d, 1H); 3.45-3.42 (m, 1H); 3.16-3.04 (m, 1H); 2.99-2.97 (m, 2H); 2.82-2.78 (m, 1H); 2.64-2.54 (m, 5H); 2.48-2.42 (m, 1H); 2.36-2.09 (m, 2H); 2.31 (s, 3H); 2.14 (s, 3H); 2.03 (s, 3H); 1.85-1.77 (m, 2H); 1.73-1.66 (m, 2H); 1.44-1.18 (m, 22H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.6, 171.5, 148.2, 145.6, 144.8, 144.5, 143.9, 141.5, 140.3, 131.7, 130.8, 129.3, 127.4, 125.6, 124.6, 121.0, 118.1, 115.0, 114.9, 114.2, 114.1, 109.9, 102.1, 64.8, 61.1, 60.3, 60.1, 59.9, 59.5, 56.1, 55.2, 54.6, 42.6, 42.1, 41.8, 39.9, 34.5, 34.1, 32.0, 31.9, 29.9, 29.6, 29.5, 29.2, 29.1, 28.9, 25.4, 24.9, 24.2, 22.8, 16.0, 14.2, 9.9.

ESI-MS m/z: Calcd. for C₄₆H₅₄N₄O₁₀S: 980.5 Found (M+H⁺): 981.5.

EXAMPLE 124

146 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 1H); 6.47 (s, 1H); 6.43 (s, 1H); 6.01 (dd, 2H); 5.66 (s, 1H); 5.39 (s, 1H); 5.02 (d, 1H); 4.55 (s, 1H); 4.31 (s, 1H); 4.26 (dd, 1H); 4.17 (d, 1H); 4.11 (dd, 1H); 3.77 (s, 3H); 3.61 (s, 3H); 3.51 (d, 1H); 3.42-3.40 (m, 1H); 3.16-3.04 (m, 1H); 2.94-2-92 (m, 2H); 2.82-2.74 (m, 1H); 2.66-2.44 (m, 2H); 2.53 (t, 2H); 2.36-2.15 (m, 2H); 2.31 (s, 3H); 2.18 (s, 3H); 2.02 (s, 3H); 1.78-1.59 (m, 4H); 1.40-1.16 (m, 25H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 148.0, 144.7, 144.5, 143.2, 141.5, 140.5, 138.7, 137.5, 131.0, 129.5, 129.3, 129.0, 125.9, 121.4, 120.9, 118.3, 114.2, 102.0, 64.8, 61.3, 60.5, 60.2, 59.9, 59.8, 55.3, 54.9, 54.8, 42.5, 42.0, 41.8, 39.9, 34.2, 32.1, 31.7, 29.9, 29.7, 29.6, 29.5, 29.4, 29.0, 25.0, 24.4, 22.8, 16.0, 14.2, 9.9.

ESI-MS m/z: Calcd. for C₅₄H₇₀N₄O₁₀S: 966.4 Found (M+H⁺): 967.5.

EXAMPLE 125

147 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 7.58 (s, 1H); 6.91 (s, 1H); 6.54 (s, 1H); 6.46 (s, 1H); 6.40 (s, 1H); 6.04 (d, 1H); 5.96 (d, 1H); 5.66 (s, 1H); 5.26 (s, 1H); 5.01 (d, 1H); 4.50-4.46 (m, 2H); 4.34 (s, 1H); 4.31-4.26 (m, 2H); 4.18 (d, 1H); 4.08 (dd, 1H); 3.74 (s, 3H); 3.60 (s, 3H); 3.51 (d, 1H); 3.40 (s, 1H); 3.17-3.08 (m, 2H); 2.92-2.80 (m, 4H); 2.74-2.35 (m, 5H); 2.28 (s, 3H); 2.17 (s, 3H); 2.02 (s, 3H); 1.80-1.70 (m, 6H).

ESI-MS m/z: Calcd. for C₄₈H₅₄N₆O₁₁S₂: 954.4 Found (M+H⁺): 955.4.

EXAMPLE 126

ESI-MS m/z: Calcd. for C₅₈H₆₈N₈O₁₃S₃: 1180.4 Found (M+H⁺): 1181.3.

EXAMPLE 127

149 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.58 (s, 1H); 6.49 (s, 1H); 6.44 (s, 1H); 5.99 (s, 1H); 5.91 (s, 1H); 5.78 (s, 1H); 5.41 (s, 1H); 5.00 (d, 1H); 4.87 (s, 1H); 4.30-4.29 (m, 2H); 4.15-4.13 (m, 2H); 3.80 (s, 3H); 3.65 (s, 3H); 3.62 (s, 3H); 3.51 (d, 1H); 3.40 (s, 1H); 3.12-3.02 (m, 1H); 2.93 (d, 2H); 2.82-2.78 (m, 1H); 2.66-2.58 (m, 1H); 2.48-2.43 (m, 1H); 2.32 (s, 3H); 2.20 (s, 3H); 2.18 (s, 3H).

ESI-MS m/z: Calcd. for C₃₉H₄₂N₄O₉S: 742.3 Found (M+H⁺): 743.3.

EXAMPLE 128

150 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.75 (s, 1H); 6.50 (s, 1H); 6.44 (s, 1H); 6.00 (s, 1H); 5.92 (s, 1H); 5.39 (s, 1H); 5.01 (d, 1H); 4.81 (s, 1H); 4.30-4.25 (m, 2H); 4.16-4.13 (m, 2H); 3.95 (s, 3H); 3.83 (s, 3H); 3.74 (s, 3H); 3.62 (s, 3H); 3.51 (d, 1H); 3.41 (s, 1H); 3.12-3.02 (m, 1H); 2.93 (d, 2H); 2.87-2.80 (m, 1H); 2.66-2.58 (m, 1H); 2.49-2.43 (m, 1H); 2.28 (s, 3H); 2.23 (s, 3H); 2.18 (s, 3H).

ESI-MS m/z: Calcd. for C₄₀H₄₄N₄O₉S: 756.3 Found (M+H⁺): 757.3.

EXAMPLE 129

151 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.58 (s, 1H); 6.49 (s, 1H); 6.44 (s, 1H); 5.99 (s, 1H); 5.91 (s, 1H); 5.75 (s, 1H); 5.00 (d, 1H); 4.90 (s, 1H); 4.30 (d, 2H); 4.17 (s, 1H); 4.15 (dd, 1H); 3.88 (q, 2H); 3.80 (s, 3H); 3.62 (s, 3H); 3.51 (d, 1H); 3.40 (s, 1H); 3.12-3.02 (m, 1H); 2.93 (d, 2H); 2.86-2.80 (m, 1H); 2.68-2.56 (m, 1H); 2.48-2.42 (m, 1H); 2.31 (s, 3H); 2.23-2.21 (m, 2H); 2.20 (s, 3H); 2.17 (s, 3H); 1.39 (t, 3H).

ESI-MS m/z: Calcd. for C₄₀H₄₄N₄O₉S: 756.3 Found (M+H⁺): 757.5

EXAMPLE 130

152 was obtained using Method F ¹H-NMR (300 MHz, CDCl₃): δ 6.76 (s, 1H); 6.50 (s, 1H); 6.44 (s, 1H); 5.99 (d, 1H); 5.92 (d, 1H); 5.42 (s, 1H); 5.001 (d, 1H); 4.87 (s, 1H); 4.35-4.27 (m, 3H); 4.18 (s, 1H); 4.16 (dd, 1H); 3.97-3.80 (m, 4H); 3.85 (s, 3H); 3.63 (s, 3H); 3.51 (d, 1H); 3.43 (s, 1H); 3.14-3.06 (m, 1H); 2.95 (d, 2H); 2.88-2.80 (m, 1H); 2.70-2.58 (m, 1H); 2.50-2.45 (m, 1H); 2.28 (s, 3H); 2.21 (s, 3H); 2.18 (s, 3H); 1.41 (t, 3H); 1.40 (t, 3H).

ESI-MS m/z: Calcd. for C₄₂H₄₈N₄O₉S: 784.3 Found (M+H⁺): 785.3.

EXAMPLE 131

153 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.58 (s, 1H); 6.49 (s, 1H); 6.43 (s, 1H); 5.98 (s, 1H); 5.91 (s, 1H); 5.70 (s, 1H); 5.40 (s, 1H); 5.01 (d, 1H); 4.90 (s, 1H); 4.30 (s, 2H); 4.17 (s, 1H); 4.15 (dd, 1H); 3.85-3.73 (m, 2H); 3.79 (s, 3H); 3.62 (s, 3H); 3.51 (d, 1H); 3.41 (s, 1H); 3.14-3.04 (m, 1H); 2.93 (d, 2H); 2.86-2.82 (m, 1H); 2.70-2.60 (m, 1H); 2.48-2.42 (m, 1H); 2.31 (s, 3H); 2.23 (s, 2H); 2.19 (s, 3H); 2.17 (s, 3H); 1.82-1.76 (m, 2H); 1.06 (t, 3H).

ESI-MS m/z: Calcd. for C₄₁H₄₆N₄O₉S: 770.3 Found (M+H⁺): 771.3.

EXAMPLE 132

154 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.76 (s, 1H); 6.50 (s, 1H); 6.43 (s, 1H); 5.98 (d, 1H); 5.91 (d, 1H); 5.40 (s, 1H); 5.01 (d, 1H); 4.88 (s, 1H); 44.32-4.12 (m, 5H); 3.85 (s, 3H); 3.82-3.59 (m, 4H); 3.62 (s, 3H); 3.51 (d, 1H); 3.43 (s, 1H); 3.14-3.06 (m, 1H); 2.94 (d, 2H); 2.87-2.80 (m, 1H); 2.71-2.60 (m, 1H); 2.49-2.44 (m, 1H); 2.27 (s, 3H); 2.21 (s, 3H); 2.17 (s, 3H); 1.82-1.67 (m, 4H); 1.07 (t, 3H); 1.02 (t, 3H).

ESI-MS m/z: Calcd. for C₄₄H₅₂N₄O₉S: 812.3 Found (M+H⁺): 813.3.

EXAMPLE 133

155 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.58 (s, 1H); 6.49 (s, 1H); 6.44 (s, 1H); 6.15-6.02 (m, 1H); 5.99 (s, 1H); 5.92 (s, 1H); 5.70 (s, 1H); 5.43 (dd, 1H); 5.26 (dd, 1H); 5.01 (d, 1H); 4.91 (s, 1H); 4.49 (dd, 1H); 4.32-4.28 (m, 2H); 4.21-4.13 (m, 3H); 3.79 (s, 3H); 3.62 (s, 3H); 3.50 (d, 1H); 3.41 (s, 1H); 3.12-3.04 (m, 1H); 2.93 (d, 2H); 2.86-2.82 (m, 1H); 2.67-2.58 (m, 1H); 2.48-2.43 (m, 1H); 2.31 (s, 3H); 2.24 (s, 2H); 2.20 (s, 3H); 2.18 (s, 3H).

ESI-MS m/z: Calcd. for C₄₁H₄₄N₄O₉S: 768.3 Found (M+H⁺): 769.2

EXAMPLE 134

156 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): S 6.77 (s, 1H); 6.49 (s, 1H); 6.43 (s, 1H); 6.15-6.01 (m, 2H); 5.99 (d, 1H); 5.92 (d, 1H); 5.43 (dd, 1H); 5.37 (dd, 1H); 5.24-5.18 (m, 2H); (dd, 1H); 5.01 (d, 1H); 4.89 (s, 1H); 4.78 (dd, 1H); 4.48-4.35 (m, 2H); 4.29-4.26 (m, 2H); 4.23-4.13 (m, 3H); 3.84 (s, 3H); 3.62 (s, 3H); 3.50 (d, 1H); 3.41 (s, 1H); 3.14-3.05 (m, 1H); 2.94 (d, 2H); 2.86-2.82 (m, 1H); 2.70-2.60 (m, 1H); 2.49-2.43 (m, 1H); 2.28 (s, 3H); 2.23 (s, 2H); 2.19 (s, 3H); 2.18 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.2, 150.8, 149.4, 149.0, 145.8, 144.7, 144.4, 138.8, 134.7, 133.6, 131.4, 130.5, 129.5, 124.7, 124.5, 122.2, 118.3, 118.0, 117.2, 114.4, 114.0, 113.2, 109.7, 101.7, 74.2, 73.3, 65.4, 61.6, 60.5, 60.3, 59.8, 59.7, 55.3, 55.2, 54.8, 42.9, 42.0, 41.9, 40.0, 29.9, 29.0, 24.5, 16.0, 9.8.

ESI-MS m/z: Calcd. for C₄₄H₄₈N₄O₉S: 808.3 Found (M+H⁺): 809.5.

EXAMPLE 135

157 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 7.53-7.50(m, 2H); 7.44-7.37 (m, 3H); 6.57 (s, 1H); 6.49 (s, 1H); 6.47 (s, 1H); 5.97 (dd, 2H); 5.56 (s, 1H); 5.02 (d, 1H); 5.00 (d, 1H); 4.87 (s, 1H); 4.76 (d, 1H); 4.31 (s, 1H); 4.20-4.14 (m, 3H); 3.76 (s, 3H); 3.64 (s, 3H); 3.41 (d, 2H); 3.13-3.05 (m, 1H); 2.92 (d, 2H); 2.84-2.78 (m, 1H); 2.69-2.58 (m, 1H); 2.49-2.42 (m, 1H); 2.35-2.04 (m, 2H); 2.31 (s, 3H); 2.25 (s, 3H); 2.17 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 72.5, 148.9, 148.0, 145.9, 144.4, 143.3, 139.0, 137.3, 131.0, 129.6, 128.6, 128.4, 128.2, 120.8, 118.4, 118.2, 114.9, 114.4, 114.2, 113.3, 109.8, 101.8, 92.6, 65.4, 61.6, 60.6, 60.4, 59.7, 55.2, 54.8, 42.9, 42.02, 41.8, 40.0, 31.8, 29.9, 24.4, 22.8, 16.0, 14.3, 9.9.

ESI-MS m/z: Calcd. for C₄₅H₄₆N₄O₉S: 818.3 Found (M+H⁺): 819.2.

EXAMPLE 136

158 was obtained using Method F ¹H-NMR (300 MHz, CDCl₃): δ 7.51-7.47 (m, 2H); 7.30-7.25 (m, 5H); 7.22-7.18 (m, 3H); 6.79 (s, 1H); 6.50 (s, 1H); 6.47 (s, 1H); 6.01 (d, 1H); 5.93 (d, 1H); 5.43 (s, 1H); 5.24 (d, 1H); 5.02 (d, 1H); 5.01 (s, 2H); 4.95 (d, 1H); 4.66 (d, 1H); 4.28 (s, 1H); 4.18-4.09 (m, 3H); 3.88 (s, 3H); 3.64 (s, 3H); 3.43 (d, 2H); 3.36-3.34 (m, 1H); 3.16-3.07 (m, 1H); 2.91 (d, 2H); 2.88-2.80 (m, 1H); 2.69-2.59 (m, 1H); 2.50-2.45 (m, 1H); 2.37-2.29 (m, 2H); 2.32 (s, 6H); 2.23 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.7, 150.8, 149.3, 148.9, 146.1, 144.9, 144.6, 139.2, 138.0, 137.3, 131.6, 131.2, 130.8, 128.7, 128.6, 128.5, 128.4, 128.3, 126.0, 125.1, 124.8, 122.6, 118.6, 114.6, 114.4, 113.6, 110.0, 101.9, 74.8, 74.6, 65.5, 61.9, 60.7, 60.1, 59.9, 55.4, 55.0, 53.8, 43.3, 42.2, 41.7, 40.1, 29.3, 24.7, 16.2, 10.0.

ESI-MS m/z: Calcd. for C₅₂H₅₂N₄O₉S: 908.3 Found (M+H⁺): 909.3.

EXAMPLE 137

Method J: To a solution of 1 equiv. of starting material in CH₃CN/CH₂Cl₂ 1.2:1 were added NaI (6 equiv.) and TMSCl (6 equiv.). After 1 h the reaction was quenched with brine, the aqueous phase was extracted with CH₂Cl₂. The organic layer was dried over Na₂SO₄. Chromatography gives pure compounds.

159 was obtained using Method J. ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 1H); 6.49 (s, 1H); 6.46 (s, 1H); 6.10 (d, 1H); 6.03 (d, 1H); 5.69 (s, 1H); 5.04 (d, 1H); 4.58 (s, 1H); 4.34 (s, 1H); 4.29 (d, 1H); 4.21 (d, 1H); 4.14 (dd, 1H); 3.76 (s, 3H); 3.63 (s, 3H); 3.50 (d, 1H); 3.43 (s, 1H); 3.20-3.08 (m, 1H); 2.95 (d, 2H); 2.90-2.84 (m, 1H); 2.78-2.72 (m, 1H); 2.91-2.48 (m, 1H); 2.34-2.03 (m, 2H); 2.31 (s, 3H); 2.20 (s, 3H); 2.06 (s, 3H).

ESI-MS m/z: Calcd. for C₄₀H₃₉F₃N₄O₁₀S: 824.2 Found (M+H⁺): 825.2.

EXAMPLE 138

160 was obtained using Method J. ¹H-NMR (300 MHz, CDCl₃): δ 6.89(s, 1H); 6.50 (s, 1H); 6.13 (d, 1H); 6.04 (d, 1H); 6.01 (s, 1H); 5.50 (s, 1H); 4.80 (d, 1H); 4.56 (s, 1H); 4.21 (s, 1H); 4.14-4.10 (m, 2H); 3.79-3.65 (m, 2H); 3.77 (s, 3H); 3.59 (s, 3H); 3.47 (s, 1H); 3.20 (d, 1H); 2.98 (d, 2H); 2.67 (t, 3H); 2.51 (d, 1H); 2.26 (s, 3H); 2.08 (s, 3H); 2.06 (s, 3H).

ESI-MS m/z: Calcd. for C₄₂H₃₈F₆N₄O₁₁S: 920.2 Found (M+H⁺): 921.3.

EXAMPLE 139

Method H: To a solution of 1 equiv. of starting material in CH₃CN/H₂O 3:2 (0.009M) were added 30 equiv. of AgNO₃. After 24 h the reaction was quenched with a mixture 1:1 of saturated solutions of brine and NaHCO₃, stirred for 10 min and diluted and extracted with CH₂Cl₂. The organic layer was dried over Na₂SO₄. Chromatography gives pure compounds.

161 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 7.89 (d, 1H); 7.60-7.56 (m, 2H); 7.46-7.44 (m, 3H); 6.57 (d, 1H); 6.56 (s, 1H); 6.48 (s, 1H); 6.44 (s, 1H); 5.99 (dd, 2H); 5.43 (s, 1H); 5.14 (d, 1H); 4.86 (s, 1H); 4.52-4.50 (m, 2H); 4.19 (d, 1H); 4.06 (dd, 1H); 3.63 (s, 3H); 3.46 (s, 3H); 3.25-3.02 (m, 3H); 2.88-2.85 (m, 3H); 2.73-2.59 (m, 1H); 2.50-2.24 (m, 3H); 2.25 (s, 3H); 2.17 (s, 3H); 2.07 (s, 3H).

ESI-MS m/z: Calcd. for C₄₆H₄₇N₃O₁₁S: 849.3 Found (M+H⁺): 850.3.

EXAMPLE 140

162 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 7.88 (d, 1H); 7.85 (d, 1H); 7.45-7.31 (m, 10H); 6.94 (s, 1H); 6.63 (d, 1H); 6.52 (d, 1H); 6.51 (s, 1H); 6.43 (s, 1H); 6.07 (s, 1H); 5.97 (s, 1H); 5.42 (s, 1H); 5.16 (d, 1H); 4.88 (s, 1H); 4.54 (s, 1H); 4.45 (s, 1H); 4.06 (d, 1H); 3.80-3.78 (m, 1H); 3.64 (s, 3H); 3.46 (s, 3H); 3.28-3.15 (m, 2H); 3.00-2.88 (m, 3H); 2.76-2.66 (m, 1H); 2.50-2.17 (m, 4H); 2.28 (s, 3H); 2.14 (s, 3H); 2.11 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.3, 164.5, 164.2, 148.0, 147.2, 146.9, 145.4, 144.5, 144.2, 143.1, 141.2, 140.7, 134.1, 133.7, 131.3, 130.9, 130.7, 129.1, 129.0, 128.9, 128.2, 128.1, 127.3, 125.6, 124.1, 121.8, 116.6, 116.1, 116.0, 114.0, 112.5, 109.7, 101.7, 81.6, 64.9, 61.1, 59.9, 57.7, 57.6, 56.1, 55.8, 54.9, 42.7, 42.5, 41.4, 39.8, 29.6, 28.7, 23.9, 22.6, 15.8, 9.7.

ESI-MS m/z: Calcd. for C₅₅H₅₃N₃O₁₂S: 979.3 Found (M+H⁺): 980.3.

EXAMPLE 141

163 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 1H); 6.47 (s, 1H); 6.43 (s, 1H); 6.02 (d, 1H); 5.93 (d, 1H); 5.64 (s, 1H); 5.12 (d, 1H); 4.81 (s, 1H); 4.47 (s, 1H); 4.15 (d, 1H); 4.03 (dd, 1H); 3.78 (s, 3H); 3.60 (s, 3H); 3.60-3.59 (m, 1H); 3.58 (d, 1H); 3.21-3.10 (m, 2H); 2.87-2.79 (m, 3H); 2.68-2.58 (m, 2H); 2.54-2.38 (m, 2H); 2.52 (t, 2H); 2.31 (s, 3H); 2.16 (s, 3H); 2.01 (s, 3H); 1.81-1.73 (m, 2H); 1.02 (t, 3H).

ESI-MS m/z: Calcd. for C₄₁H₄₇N₃O₁₁S: 789.3 Found (M+H⁺): 790.1.

EXAMPLE 142

164 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 7.96 (s, 1H); 6.47 (s, 1H); 6.42 (s, 1H); 6.02 (d, 1H); 5.93 (d, 1H); 5.40 (s, 1H); 5.12 (d, 1H); 4.81 (s, 1H); 4.47 (s, 1H); 4.18-4.16 (m, 1H); 4.03 (d, 1H); 3.78 (s, 3H); 3.71-3.70 (m, 2H); 3.61 (s, 3H); 3.23-3.10 (m, 2H); 2.87-2.79 (m, 3H); 2.68-2.40 (m, 3H); 2.60 (t, 2H); 2.31 (s, 3H); 2.16 (s, 3H); 2.01 (s, 3H); 1.84-1.73 (m, 4H); 1-09 (t, 3H); 1.03 (t, 3H).

ESI-MS m/z: Calcd. for C₄₅H₅₃N₃O₁₂S: 859.3 Found (M+H⁺): 860.3.

EXAMPLE 143

165 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 1H); 6.47 (s, 1H); 6.45 (s, 1H); 6.03 (d, 1H); 5.98-5.85 (m, 1); 5.95 (d, 1H); 5.70 (s, 1H); 5.37 (dd, 1H); 5.26 (dd, 1H); 5.12 (d, 1H); 4.80 (s, 1H); 4.64-4.62 (m, 2H); 4.58 (s, 1H); 4.48 (d, 1H); 4.17 (d, 1H); 4.05 (dd, 1H); 3.77 (s, 3H); 3.60 (s, 3H); 3.57 (d, 1H); 3.22-3.10 (m, 2H); 2.87-2.78 (m, 3H); 2.68-2.58 (m, 1H); 2.49-2.20 (m, 2H); 2.31 (s, 3H); 2.17 (s, 3H); 2.08 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.7, 152.7, 147.9, 145.3, 144.6, 144.4, 143.1, 141.3, 140.9, 131.5, 129.4, 129.2, 126.2, 122.3, 121.0, 119.0, 116.1, 114.2, 112.6, 109.9, 101.9, 82.3, 69.3, 64.7, 61.4, 60.5, 57.9, 57.8, 56.2, 55.3, 55.0, 42.5, 42.0, 41.6, 39.8, 29.9, 28.9, 24.2, 16.0, 9.5.

ESI-MS m/z: Calcd. for C₄₁H₄₅N₃O₁₂S: 803.3 Found (M+H⁺): 804.3.

EXAMPLE 144

166 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 6.60 (s, 1H); 6.47 (s, 1H); 6.32 (s, 1H); 6.03 (d, 1H); 5.95 (d, 1H); 5.72 (s, 1H); 5.12 (d, 1H); 4.82 (s, 1H); 4.48 (d, 1H); 4.43 (s, 1H); 4.17-4.14 (m, 1H); 4.04 (dd, 1H); 3.85 (ddd, 2H); 3.79 (s, 3H); 3.61 (s, 3H); 3.60-3.57 (m, 1H); 3.24-3.10 (m, 2H); 3.03 (t, 2H); 2.88-2.78 (m, 3H); 2.68-2.56 (m, 1H); 2.49-2.43 (m, 1H); 2.38-2.13 (m, 2H); 2.31 (s, 3H); 2.17 (s, 3H); 2.04 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.6, 167.8, 147.8, 145.4, 144.6, 144.4, 143.2, 141.1, 140.9, 131.6, 129.3, 126.1, 121.8, 114.2, 109.9, 101.9, 82.2, 64.7, 61.5, 60.6, 58.0, 57.8, 56.1, 55.3, 55.1, 42.5, 42.3, 41.6, 39.9, 38.8, 37.7, 29.9, 29.5, 29.0, 24.3, 22.9, 16.0, 14.3, 9.9.

ESI-MS m/z: Calcd. for C₄₀H₄₄ClN₃O₁₁S: 809.2 Found (M+H⁺): 810.3.

EXAMPLE 145

167 was obtained using Method H ¹H-NMR (300 MHz, CDCl₃): S 6.60 (s, 1H); 6.49 (s, 1H); 6.46 (s, 1H); 6.07 (s, 1H); 6.00 (s, 1H); 5.64 (s, 1H); 5.39 (s, 1H); 5.16 (d, 1H); 4.83 (s, 1H); 4.49 (s, 1H); 4.19-4.18 (m, 1H); 4.06 (dd, 1H); 3.76 (d, 1H); 3.62 (s, 3H); 3.57-3.56 (m, 1H); 3.24-3.12 (m, 2H); 2.89-2.85 (m, 2H); 2.79-2.73 (m, 1H); 2.68-2.58 (m, 1H); 2.52-2.45 (m, 1H); 2.37-2.10 (m, 2H); 2.31 (s, 3H); 2.18 (s, 3H); 2.03 (s, 3H).

ESI-MS m/z: Calcd. for C₄₁H₄₀F₇N₃O₁₁S: 915.2 Found (M+H⁺): 916.2.

EXAMPLE 146

168 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 6.60 (s, 1H); 6.47 (s, 1H); 6.43 (s, 1H); 5.97 (dd, 2H); 5.64 (s, 1H); 5.32 (s, 1H); 5.12 (d, 1H); 4.81 (s, 1H); 4.48 (s, 1H); 4.48-4.45 (m, 1H); 4.16 (d, 1H); 4.03 (dd, 1H); 3.78 (s, 3H); 3.60 (s, 3H); 3.58 (d, 1H); 3.24-3.08 (m, 2H); 2.94-2.78 (m, 3H); 2.66-2.42 (m, 2H); 2.53 (t, 2H); 2.38-2.12 (m, 2H); 2.31 (s, 3H); 2.16 (s, 3H); 2.01 (s, 3H); 1.80-1.68 (m, 2H); 1.42-1.23 (m, 11H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.6, 171.3, 147.8, 145.3, 144.6, 144.4, 143.1, 141.5, 140.6, 131.6, 129.3, 129.2, 121.9, 121.1, 114.2, 110.0, 101.8, 82.3, 64.9, 61.6, 60.5, 58.0, 57.9, 56.1, 55.2, 55.1, 42.3, 41.6, 39.9, 34.2, 31.9, 29.9, 29.6, 29.2, 25.1, 24.3, 22.8, 16.0, 14.3, 9.9.

ESI-MS m/z: Calcd. for C₄₅H₅₅N₃O₁₁S: 845.4 Found (M+H⁺): 846.7.

EXAMPLE 147

169 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 6.94 (s, 1H); 6.47 (s, 1H); 6.41 (s, 1H); 6.03 (s, 1H); 5.94 (s, 1H); 5.12 (d, 1H); 4.81 (s, 1H); 4.49 (s, 1H); 4.37 (s, 1H); 4.03 (d, 1H); 3.74 (s, 3H); 3.67-3.57 (m, 2H); 3.60 (s, 3H); 3.24-3.10 (m, 2H); 2.92-2.80 (m, 3H); 2.68-2.44 (m, 2H); 2.61 (t, 2H); 2.56 (t, 2H); 2.38-2.18 (m, 2H); 2.31 (s, 3H); 2.12 (s, 3H); 2.02 (s, 3H); 1.84-1.68 (m, 4H); 1.42-1.20 (m, 22H).

ESI-MS m/z: Calcd. for C₅₃H₆₉N₃O₁₂S: 971.5 Found (M+H⁺): 972.7.

EXAMPLE 148

170 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 1H); 6.47 (s, 1H); 6.43 (s, 1H); 6.01 (dd, 2H); 5.66 (s, 1H); 5.39 (s, 1H); 5.02 (d, 1H); 4.55 (s, 1H); 4.31 (s, 1H); 4.26 (dd, 1H); 4.17 (d, 1H); 4.11 (dd, 1H); 3.77 (s, 3H); 3.61 (s, 3H); 3.51 (d, 1H); 3.42-3.40 (m, 1H); 3.16-3.04 (m, 1H); 2.94-2.92 (m, 2H); 2.82-2.74 (m, 1H); 2.66-2.44 (m, 2H); 2.53 (t, 2H); 2.36-2.15 (m, 2H); 2.31 (s, 3H); 2.18 (s, 3H); 2.02 (s, 3H); 1.78-1.59 (m, 2H); 1.40-1.16 (m, 27H).

ESI-MS m/z: Calcd. for C₅₃H₇₁N₃O₁₁S: 957.5 Found (M+H⁺): 958.4.

EXAMPLE 149

Compound 147 was recovered (19%) after chromatographic purification.

171 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 7.50 (s, 1H); 6.81 (s, 1H); 6.56 (s, 1H); 6.45 (s, 1H); 6.40 (s, 1H); 6.02 (d, 1H); 5.93 (d, 1H); 5.21 (s, 1H); 5.12 (d, 1H); 4.84 (s, 1H); 4.51-4.46 (m, 2H); 4.41 (s, 1H); 4.32-4.21 (m, 3H); 4.01 (dd, 1H); 3.75 (s, 3H); 3.75-3.71 (m, 1H); 3.65 (s, 3H); 3.59 (s, 3H); 3.23 (s, 1H); 3.17-3.10 (m, 2H); 2.89-2.80 (m, 3H); 2.74-2.37 (m, 4H); 2.29 (s, 3H); 2.17 (s, 3H); 2.00 (s, 3H); 1.80-1.68 (m, 4H); 1.55-1.39(m, 2H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.6, 171.4, 164.5, 148.4, 145.4, 144.7, 144.6, 143.4, 141.5, 140.7, 131.1, 129.2, 129.0, 122.0, 120.6, 116.2, 114.3, 110.1, 101.9, 82.1, 70.7, 65.0, 62.4, 61.8, 60.5, 60.3, 58.1, 57.9, 56.1, 55.2, 55.0, 42.5, 41.6, 40.8, 40.1, 33.7, 32.1, 29.9, 29.5, 28.7, 28.2, 24.7, 24.3, 16.1, 14.3, 9.9.

ESI-MS m/z: Calcd. for C₄₇H₅₅N₅O₁₂S₂: 945.3 Found (M−H₂O+H⁺): 928.3.

EXAMPLE 150

172 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 6.94 (s, 1H); 6.46 (s, 1H); 6.39 (s, 1H); 6.26 (s, 1H); 6.02 (d, 1H); 5.94 (d, 1H); 5.57-5.55 (m, 2H); 5.11 (d, 1H); 4.82 (s, 1H); 4.48-4.45 (m, 3H); 4.32-4.22 (m, 3H); 4.01 (dd, 1H); 3.75 (s, 3H); 3.75-3.71 (m, 1H); 3.67-3.64 (m, 6H); 3.59 (s, 3H); 3.25-3.24 (m, 1H); 3.19-3.10 (m, 3H); 2.92-2.83 (m, 4H); 2.74-2.60 (m, 6H); 2.46-2.14 (m, 2H); 2.31 (s, 3H); 2.11 (s, 3H); 2.03 (s, 3H); 1.91-1.66 (m, 8H); 1.59-1.44 (m, 4H).

ESI-MS m/z: Calcd. for C₄₇H₅₅N₅O₁₂S₂: 1171.4 Found (M−H₂O+H⁺): 1154.3.

EXAMPLE 151

173 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 6.69 (s, 1H); 6.60 (s, 1H); 6.59 (s, 1H); 6.00 (s, 1H); 5.92 (s, 1H); 5.66 (s, 1H); 5.11 (d, 1H); 4.78 (s, 1H); 4.59 (s, 1H); 4.46 (d, 1H); 4.15 (d, 1H); 4.04 (dd, 1H); 3.79 (s, 3H); 3.57 (s, 3H); 3.56-3.52 (m, 1H); 3.21-3.09 (m, 2H); 2.87-2.75 (m, 3H); 2.69-2.38 (m, 3H); 2.31 (s, 3H); 2.30-2.10 (m, 2H); 2.16 (s, 3H); 2.06 (s, 3H); 1.50 (s, 9H); 1.48 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.2, 151.8, 150.9, 148.6, 147.9, 145.3, 143.1, 141.3, 140.6, 138.9, 133.1, 131.7, 129.3, 128.8, 122.3, 121.0, 118.1, 115.9, 112.7, 112.1, 101.8, 83.6, 83.3, 82.3, 65.1, 61.6, 60.4, 57.9, 56.2, 55.4, 55.1, 42.5, 42.0, 41.6, 39.7, 29.9, 28.8, 27.9, 27.8, 24.3, 16.0, 9.5.

ESI-MS m/z: Calcd. for C₄₇H₅₇N₃O₁₄S: 919.4 Found (M+H⁺): 920.3

174 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 6.92 (s, 1H); 6.69 (s, 1H); 6.58 (s, 1H); 6.01 (s, 1H); 5.93 (s, 1H); 5.10 (d, 1H); 4.76 (s, 1H); 4.55 (s, 1H); 4.46 (d, 1H); 4.04 (dd, 1H); 3.84 (d, 1H); 3.81 (s, 3H); 3.61-3.58 (m, 1H); 3.58 (s, 3H); 3.24-3.10 (m, 2H); 2.99-2.77 (m, 3H); 2.70-2.60 (m, 1H); 2.51-2.17 (m, 3H); 2.30 (s, 3H); 2.14 (s, 3H); 2.07 (s, 3H); 1.55 (s, 9H); 1.51 (s, 9H); 1.49 (s, 9H).

ESI-MS m/z: Calcd. for C₅₂H₆₅N₃O₁₆S: 1019.4 Found (M+H⁺): 1020.4

EXAMPLE 153

175 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 6.69 (s, 1H); 6.57 (s, 1H); 6.55 (s, 1H); 6.02 (d, 1H); 5.94 (d, 1H); 5.12 (d, 1H); 5.02 (d, 1H); 4.82 (s, 1H); 4.61 (t, 1H); 4.49 (d, 1H); 4.41 (s, 1H); 4.17 (d, 1H); 4.00 (dd, 1H); 3.77 (s, 3H); 3.57-3.55 (m, 1H); 3.56 (s, 3H); 3.22-3.09 (m, 2H); 2.86-2.80 (m, 3H); 2.69-2.60 (m, 1H); 2.50-2.36 (m, 2H); 2.30 (s, 3H); 2.15 (s, 3H); 2.01 (s, 3H); 1.61 (d, 3H); 1.50 (s, 9H); 1.43 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.2, 171.3, 155.5, 151.8, 148.7, 147.9, 145.5, 143.3, 140.9, 139.0, 132.8, 131.7, 129.6, 128.8, 122.4, 122.0, 120.9, 118.1, 116.2, 112.1, 102.0, 83.6, 82.1, 65.3, 61.5, 60.6, 58.0, 56.2, 55.4, 54.9, 49.3, 42.4, 41.6, 39.9, 29.9, 28.9, 28.5, 27.8, 24.2, 18.6, 16.0, 9.8.

ESI-MS m/z: Calcd. for C₅₀H₆₂N₄O₁₅S: 990.4 Found (M+H⁺): 991.4.

EXAMPLE 154

176 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 6.99 (dd, 1H); 6.69 (s, 1H); 6.60 (s, 1H); 6.59 (s, 1H); 6.03 (d, 1H); 5.95 (d, 1H); 5.70 (s, 1H); 5.12 (d, 1H); 4.97 (dd, 1H); 4.80 (s, 1H); 4.60 (dd, 1H); 4.56 (s, 1H); 4.48 (d, 1H); 4.18 (d, 1H); 4.04 (dd, 1H); 3.76 (s, 3H); 3.58 (s, 3H); 3.58-3.56 (m, 1H); 3.47 (d, 1H); 3.24-3.12 (m, 2H); 2.87-2.78 (m, 3H); 2.68-2.58 (m, 1H); 2.52-2.47 (m, 1H); 2.43-2.20 (m, 2H); 2.31 (s, 3H); 2.18 (s, 3H); 2.08 (s, 3H); 1.50 (s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.3, 151.8, 150.5, 148.7, 148.0, 145.4, 143.1, 141.1, 140.9, 139.0, 133.1, 131.6, 129.4, 128.8, 122.4, 122.3, 120.9, 116.1, 112.6, 112.0, 102.0, 98.6, 86.6, 82.2, 64.8, 61.4, 60.5, 57.9, 57.7, 56.2, 55.5, 55.0, 42.5, 42.0, 41.6, 39.7, 29.9, 28.8, 27.8, 24.1, 16.0, 9.5.

ESI-MS m/z: Calcd. for C₄₅H₅₁N₃O₀₄S: 889.3 Found (M+H⁺): 890.2

EXAMPLE 155

Method I: To a solution of 1 equiv. of starting material in THF/H₂O 4:1 (0.009M) were added 5 equiv. of BrCu. After 24 h the reaction was quenched with NH₄Cl, diluted with CH₂Cl₂, washed with brine and NaHCO₃ and extracted with CH₂Cl₂. The organic layer was dried over Na₂SO₄. Chromatography gives pure compounds.

177 was obtained using Method I. ESI-MS m/z: Calcd. for C₃₉H₄₅N₃O₁₀S: 747.3 Found (M+H⁺): 748.1.

EXAMPLE 156

178 was obtained using Method I. ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 1H); 6.49 (s, 1H); 6.44 (s, 1H); 5.96 (s, 1H); 5.87 (s, 1H); 5.67 (s, 1H); 5.12 (d, 1H); 4.85 (s, 1H); 4.78 (s, 1H); 4.49 (s, 1H); 4.20-4.18 (m, 1H); 4.08 (dd, 1H); 3.79 (s, 3H); 3.61 (s, 3H); 3.23-3.10 (m, 2H); 2.87-2.80 (m, 2H); 2.70-2.58 (m, 1H); 2.49-2.42 (m, 1H); 2.31 (s, 3H); 2.26-2.22 (m, 2H); 2.18 (s, 3H); 2.15 (s, 3H).

ESI-MS m/z: Calcd. for C₄₀H₄₇N₃O₁₀S: 761.3 Found (M+H⁺): 762.3.

EXAMPLE 157

179 was obtained using Method I. ¹H-NMR (300 MHz, CDCl₃): δ 6.79 (s, 1H); 6.50 (s, 1H); 6.45 (s, 1H); 6.15-6.02 (m, 2H); 5.97 (d, 1H); 5.88 (d, 1H); 5.46-5.35 (m, 3H); 5.20 (dd, 2H); 5.13 (d, 1H); 4.84 (s, 1H); 4.78-4.74 (m, 2H); 4.49-4.38 (m, 3H); 4.21-4.08 (m, 3H); 3.84 (s, 3H); 3.62 (s, 3H); 3.57 (d, 1H); 3.49 (s, 1H); 3.22-3.08 (m, 2H); 2.92-2.82 (m, 3H); 2.72-2.60 (m, 1H); 2.52-2.46 (m, 1H); 2.28 (s, 3H); 2.26-2.23 (m, 2H); 2.17 (s, 6H).

ESI-MS m/z: Calcd. for C₄₃H₄₉N₃O₁₀S: 799.3 Found (M+H⁺): 800.2.

EXAMPLE 158

180 was obtained using Method I. ¹H-NMR (300 MHz, CDCl₃): δ 7.54-7.51 (m, 2H); 7.40-7.29 (m, 3H); 6.58 (s, 1H); 6.49 (s, 1H); 6.48 (s, 1H); 5.99 (d, 1H); 5.91 (d, 1H); 5.34 (s, 1H); 5.14 (d, 1H); 5.01 (d, 1H); 4.84 (s, 1H); 4.79 (s, 1H); 4.72 (d, 1H); 4.49 (d, 1H); 4.12-4.07 (m, 2H); 3.77 (s, 3H); 3.64 (s, 3H); 3.50 (d, 1H); 3.22-3.10 (m, 2H); 2.87-2.82 (m, 2H); 2.70-2.60 (m, 1H); 2.49-2.43 (m, 1H); 2.34-2.10 (m, 2H); 2.31 (s, 3H); 2.24 (s, 3H); 2.15 (s, 3H).

ESI-MS m/z: Calcd. for C₄₄H₄₇N₃O₁₀S: 809.3 Found (M+H⁺): 810.3.

EXAMPLE 159

181 was obtained using Method I. ESI-MS m/z: Calcd. for C₅₁H₅₃N₃O₁₀S: 899.4 Found (M+H⁺): 900.3.

EXAMPLE 160

Method K: To a solution of 1 equiv. of starting material in THF/H₂O 4:1 (0.009M) were added 5 equiv. of ClCu. After 24 h the reaction was quenched with NH₄Cl, diluted with CH₂Cl₂, washed with brine and NaHCO₃ and extracted with CH₂Cl₂. The organic layer was dried over Na₂SO₄. Chromatography gives pure compounds.

182 was obtained using Method I. ¹H-NMR (300 MHz, CDCl₃): δ 6.60 (s, 1H); 6.49 (s, 1H); 6.45 (s, 1H); 5.97 (s, 1H); 5.88 (s, 1H); 5.76 (s, 1H); 5.11 (d, 1H); 4.80 (s, 1H); 4.48-4.46 (m, 1H); 4.20-4.18 (m, 1H); 4.07 (dd, 1H); 3.80 (s, 3H); 3.74 (s, 3H); 3.74-3.60 (m, 2H); 3.61 (s, 3H); 3.22-3.08 (m, 2H); 2.87-2.78 (m, 3H); 2.66-2.58 (m, 1H); 2.49-2.44 (m, 1H); 2.32 (s, 3H); 2.31-2.24 (m, 2H); 2.18 (s, 3H); 2.17 (s, 3H).

ESI-MS m/z: Calcd. for C₃₈H₄₃N₃O₁₀S: 733.3 Found (M+H⁺): 734.2.

EXAMPLE 161

183 was obtained using Method I. ¹H-NMR (300 MHz, CDCl₃): δ 6.59 (s, 1H); 6.49 (s, 1H); 6.45 (s, 1H); 6.15-6.02 (m, 1H); 5.97 (d, 1H); 5.88 (d, 1H); 5.69 (s, 1H); 5.43 (dd, 1H); 5.24 (dd, 1H); 5.12 (d, 1H); 4.85 (s, 1H); 4.78 (s, 1H); 4.52-4.47 (m, 2H); 4.21-4.15 (m, 2H); 4.08 (dd, 1H); 3.80 (s, 3H); 3.64-3.57 (m, 2H); 3.61 (s, 3H); 3.22-3.20 (m, 1H); 3.16-3.08 (m, 1H); 2.87-2.80 (m, 3H); 2.68-2.58 (m, 1H); 2.49-2.43 (m, 1H); 2.31 (s, 3H); 2.26 (d, 2H); 2.18 (s, 3H); 2.17 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.5, 149.4, 147.9, 145.6, 144.6, 144.4, 143.2, 139.2, 134.0, 129.5, 122.9, 121.0, 117.5, 115.9, 114.3, 112.4, 109.8, 101.8, 82.3, 74.1, 65.4, 61.7, 60.6, 58.4, 58.0, 56.5, 55.2, 55.1, 43.1, 42.3, 41.6, 40.0, 29.9, 29.5, 29.1, 24.4, 22.9, 16.0, 14.3, 9.8.

ESI-MS m/z: Calcd. for C₄₀H₄₅N₃O₁₀S: 759.3 Found (M+H⁺): 760.3.

EXAMPLE 162

To a solution of Et-743 in MeOH (0.19M) were added 15 equiv. of KOH. The reaction mixture was stirred at room temperature for 1 h 30 minutes. After this time the reaction was quenched with NH₄Cl, diluted and extracted with CH₂Cl₂. The organic layer was dried over Na₂SO₄. Chromatography gives pure Et-701.

Et-701 ¹H-NMR (300 MHz, CDCl₃): δ 6.60 (s, 1H); 6.47 (s, 1H); 6.40 (s, 1H); 5.93 (d, 2H); 5.84 (d, 1H); 5.08 (d, 1H); 4.82 (s, 1H); 4.46 (d, 1H); 4.43 (d, 1H); 4.18 (d, 1H); 3.97 (dd, 1H); 3.70 (s, 3H); 3.65 (d, 1H); 3.57 (s, 3H); 3.23-3.08 (m, 2H); 2.88-2.78 (m, 3H); 2.65-2.55 (m, 1H); 2.49-2.36 (m, 2H); 2.30 (s, 3H); 2.14 (s, 3H); 2.13 (s, 3H).

ESI-MS m/z: Calcd. for C₃₇H₄₁N₃O₁₀S: 719.3 Found (M−H₂O+H⁺): 702.2.

EXAMPLE 163

To a solution of ET-729 in MeOH (0.005M) at room temperature under Argon, were added 30 equiv. of KCN. The reaction mixture was stirred for 6 h. After this time the reaction was diluted with CH₂Cl₂, washed with NaCl, extracted with CH₂Cl₂. The organic layers were dried over Na₂SO₄. Flash chromatography gives pure compound 184 (20%).

184. ¹H-NMR (300 MHz, CDCl₃): δ 6.64 (s, 1H), 6.50 (s, 1H), 6.39 (s, 1H), 5.94 (d, 2H), 5.42 (bs, 1H), 5.00 (d, 1H), 4.54 (d, 1H), 4.48 (s, 1H), 4.36 (s, 1H), 4.19 (d, 1H), 4.04 (dd 1H), 3.88-3.83 (m, 1H), 3.78 (s, 3H), 3.60 (bs, 4H), 3.17-3.06 (m, 2H), 2.99 (dd, 1H), 2.82-2.74 (m, 1H), 2.66-2.55 (m, 1H), 2.54-2.04 (m, 3H), 2.34 (s, 3H), 2.16 (s, 3H).

ESI-MS m/z: Calcd. for C₃₇H₃₈N₄O₉S: 714.2. Found (M+H⁺): 715.2.

EXAMPLE 164

To a solution of ET-729 in acetonitrile (0.016M) at room temperature under Argon, were added 200 equiv. of formaline and 10 equiv. of NaBH₃CN. The reaction mixture was stirred for 1 h, then acetic acid (40 equiv.) was added and the reaction was left for 1 hour more. After this time the reaction was diluted with CH₂Cl₂, a saturated aqueous solution of NaHCO₃ was added and the aqueous phase was extracted with CH₂Cl₂. The organic layers were dried over Na₂SO₄. Flash chromatography gives pure compound 185 (60%).

185. ¹H-NMR (300 MHz, CD₃OD): δ 6.40 (s, 1H), 6.35 (s, 1H), 6.23 (s, 1H), 6.06 (d, 2H), 5.01 (d, 1H), 4.63 (bs, 1H), 4.26 (d, 1H), 3.88-3.85 (m, 2H), 3.74 (s, 3H), 3.52 (s, 3H), 3.32-3.11 (m, 4H), 3.00-2.79 (m, 3H), 2.66-2.51 (m, 3H), 2.50-2.20 (m, 2H), 2.33 (s, 3H), 2.24 (s, 3H), 2.20 (s, 3H), 2.12 (s, 3H), 2.03 (s, 3H).

ESI-MS m/z: Calcd. for C₄₀H₄₅N₃O₁₀S: 759.3. Found (M+H⁺): 760.2.

EXAMPLE 165

To a solution of ET-729 in MeOH (0.005M) at room temperature under Argon, were added 4.2 equiv. of KCN and 4.2 equiv. of acetic acid. The reaction mixture was stirred for 1 h 30 min. After this time the reaction was diluted with CH₂Cl₂, quenched with NaHCO₃, extracted with CH₂Cl₂. The organic layers were dried over Na₂SO₄. Flash chromatography gives pure compound 186 (93%).

186. ¹H-NMR (300 MHz, CDCl₃): δ 6.60 (s, 1H), 6.43 (s, 1H), 6.42 (s, 1H), 6.00 (d, 2H), 5.96 (bs, 1H), 5.01 (d, 1H), 4.55 (bs, 1H), 4.49 (d, 1H), 4.32 (s, 1H), 4.18 (d, 1H), 4.10 (dd 1H), 3.82 (bd, 1H), 3.74 (s, 3H), 3.57 (s, 3H), 3.50 (d, 1H), 3.12-2.92 (m, 3H), 2.79-2.75 (m, 1H), 2.61-2.53 (m, 1H), 2.46-2.41 (m, 1H), 2.37-2.03 (m, 2H), 2.30 (s, 3H), 2.24 (s, 3H), 2.03 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.5, 168.1, 145.7, 145.2, 144.5, 144.3, 142.7, 141.2, 140.0, 131.2, 129.4, 129.0, 125.5, 124.3, 121.2, 121.0, 118.0, 114.1, 113.8, 113.3, 109.8, 101.8, 64.5, 61.1, 60.2, 59.8, 58.9, 58.7, 55.0, 48.5, 47.5, 42.0, 41.8, 39.6, 28.7, 28.0, 20.3, 15.6, 9.6.

ESI-MS m/z: Calcd. for C₃₉H₄₀N₄O₁₀S: 756.2. Found (M+H⁺): 757.2.

EXAMPLE 166

To a solution of 1 equiv. of compound 186 in CH₂Cl₂ (0.036M) under Argon at room temperature, were added 40 equiv. of Pyr, 20 equiv. of Allyl chloroformate and a catalityc amount of DMAP in small portions during 26 h. Then the reaction was quenched with water/ice. The aqueous layer was extracted with CH₂Cl₂ and the organic layer was dried over Na₂SO₄. Flash cromatography gives pure compound 187 (88%).

187. ¹H-NMR (300 MHz, CDCl₃): δ 6.72 (s, 1H), 6.60 (s, 1H), 6.56 (bs, 1H), 6.02 (d, 2H), 6.04-5.76 (m, 2H), 5.69-5.57 (m, 1H), 5.42-4.97 (m, 6H), 4.69-4.49 (m, 5H), 4.34-4.29 (m, 1H), 4.22-4.09 (m, 2H), 3.78 (s, 3H), 3.57 (s, 3H), 3.78-3.48 (m, 2H), 3.22-3.05 (m, 3H), 2.89-2.43 (m, 3H), 2.36-2.16 (m, 2H), 2.31 (s, 3H), 2.29 (s, 3H), 2.05, 2.04 (2s, 3H).

ESI-MS m/z: Calcd. for C₄₇H₄₈N₄O₁₄S: 924.3. Found (M+H⁺): 925.3.

EXAMPLE 167

Method A: To a solution of 1 equiv. of starting material in CH₂Cl₂ (0.032M) under Argon were added 2 equiv. of the anhydride and 2 equiv. of base. The reaction was followed by TLC and quenched with NaHCO₃, extracted with CH₂Cl₂ and the organic layers dried over Na₂SO₄. Flash chromatography gives pure compounds.

Compound 188 is obtained with 1.5 equiv. of ((CH₃)₃COCO)₂O without base in CH₃CN). Compounds 189 and 190 are obtained with 1 equiv. of ((CH₃)₃COCO)₂O and 4 equiv. of ^(i)Pr₂NEt in CH₃CN. The ratio of these two compounds can be modified using other experimental conditions (reaction time and equiv. of reagents); even compound 190 can be obtained (78%) after 5 days when the reaction is performed with 7 equiv. of (CH₃)₃COCO)₂O and 21 equiv. of ^(i)Pr₂NEt.

188: ¹H-NMR (300 MHz, CDCl₃): δ 6.58 (s, 1H), 6.46 (s, 1H), 6.45, 6.43 (2s, 1H), 6.36, 5.80 (bs, s, 1H), 6.05-5.97 (m, 2H), 5.79, 5.44 (2d, 1H), 5.48 (bs, 1H), 5.05-4.94 (m, 2H), 4.67, 4.61 (2bs, 1H), 4.31 (s, 1H), 4.23-4.10 (m, 2H), 3.76, 3.75 (2s, 3H), 3.61 (s, 3H), 3.52-3.46 (m, 1H), 3.18-3.05 (m, 3H), 2.78-2.04 (m, 5H), 2.29 (s, 3H), 2.27 (s, 3H), 2.04, 1.98 (2s, 3H), 1.46, 1.32 (2s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.8, 172.4, 168.1, 154.5, 152.9, 146.9, 145.9, 145.3, 144.9, 144.5, 144.3, 143.2, 142.7, 141.2, 141.1, 140.0, 139.6, 131.0, 130.4, 130.1, 129.7, 129.0, 128.9, 125.5, 125.3, 121.6, 121.3, 121.1, 121.0, 120.6, 120.0, 116.8, 116.4, 114.1, 113.6, 113.3, 109.8, 101.7, 81.1, 80.7, 64.3, 61.2, 60.8, 60.2, 60.1, 59.9, 59.3, 58.3, 58.2, 58.1, 57.4, 55.0, 48.4, 48.2, 47.2, 45.8, 42.0, 41.7, 41.4, 39.6, 39.4, 28.6, 28.0, 27.9, 27.2, 20.7, 20.2, 15.7, 14.0, 9.6, 9.4.

ESI-MS m/z: Calcd. for C₄₄H₄₈N₄O₁₂S: 856.3. Found (M+H⁺): 857.2.

189: ¹H-NMR (300 MHz, CDCl₃): δ 6.68 (s, 1H), 6.61 (s, 1H), 6.57 (s, 1H), 6.01 (dd, 2H), 5.78 (bs, 1H), 5.02 (d, 1H), 4.54 (bs, 1H), 4.50 (d, 1H), 4.35 (s, 1H), 4.18 (d 1H), 4.09 (dd, 1H), 3.87-3.82 (m, 1H), 3.77 (s, 3H), 3.58 (s, 3H), 3.53 (bd, 1H), 3.13-3.07 (m, 2H), 2.98 (dd, 1H), 2.83-2.75 (m, 1H), 2.68-2.57 (m, 1H), 2.52-2.43 (m, 1H), 2.37-2.16 (m, 2H), 2.30 (s, 3H), 2.27 (s, 3H), 2.03 (s, 3H), 1.50 (s, 9H).

ESI-MS m/z: Calcd. for C₄₄H₄₈N₄O₁₂S: 856.3. Found (M+H⁺): 857.3.

190: ¹H-NMR (300 MHz, CDCl₃): δ 6.69 (s, 1H), 6.59-6.56 (m, 2H), 6.05-5.97 (m, 2H), 5.93, 5.77 (2s, 1H), 5.68, 5.43 (2d, 1H), 5.04-4.99 (m, 2H), 4.64-4.58 (m, 1H), 4.32-4.08 (m, 3H), 3.77 (s, 3H), 3.59 (s, 3H), 3.47-3.44 (m, 1H), 3.11-3.06 (m, 3H), 2.83-2.02 (m, 11H), 2.04, 2.02 (2s, 3H), 1.50, 1.45, 1.33 (3s, 18H).

ESI-MS m/z: Calcd. for C₄₉H₅₆N₄O₁₄S: 956.3. Found (M+H⁺): 957.2.

EXAMPLE 168

Compound 191 is obtained using 3 equiv. of acetic anhydride as the anhydride and 5 equiv. of pyr as base (Method A).

191. ¹H-NMR (300 MHz, CDCl₃): δ 6.61, 6.60 (2s, 1H), 6.57, 6.56 (2s, 2H), 6.40, 5.81 (bs, s, 1H), 6.04-5.97 (m, 2H), 5.79, 5.44 (2d, 1H), 5.05-5.00 (m, 1H).4.94-4.90 (m, 1H), 4.67, 4.60 (2bs, 1H), 4.31 (s, 1H), 4.22-4.08 (m, 2H), 3.77, 3.76 (2s, 3H), 3.55 (s, 3H), 3.51-3.46 (m, 1H), 3.18-3.10 (m, 3H), 2.79-2.72 (m, 1H), 2.66-2.56 (m, 1H), 2.51-2.45 (m, 1H), 2.39-2.03 (m, 2H), 2.29 (s, 3H), 2.28, 2.27 (2s, 3H), 2.24 (s, 3H), 2.03, 1.97 (2s, 3H), 1.46, 1.32 (2s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.3, 172.1, 169.0, 168.1, 156.6, 152.9, 148.4, 146.6, 145.9, 145.2, 143.2, 142.8, 141.4, 138.6, 132.5, 131.2, 130.7, 130.0, 129.8, 128.7, 122.5, 121.7, 121.3, 120.8, 120.5, 116.6, 116.4, 113.4, 111.8, 101.9, 81.2, 80.9, 64.7, 61.2, 60.9, 60.3, 60.1, 59.8, 58.4, 58.2, 57.9, 55.1, 48.5, 48.2, 47.3, 45.9, 42.3, 41.5, 39.6, 39.5, 28.6, 28.3, 28.2, 28.1, 27.4, 20.6, 20.4, 15.8, 9.7.

ESI-MS m/z: Calcd. for C₄₆H₅₀N₄O₁₃S: 898.3. Found (M+H⁺): 899.3.

EXAMPLE 169

Method B: To a solution of 1 equiv. of starting material in CH₂Cl₂ (0.032M) under Argon at room temperature were added 2 equiv. of base and 2 equiv. of the acid chloride. The reaction was followed by TLC and quenched with NaHCO₃, extracted with CH₂Cl₂ and the organic layers dried over Na₂SO₄. Flash chromatography gives pure compounds.

Compound 192 is obtained with 2.5 equiv. of butyryl chloride and 3.5 equiv. of pyridine. Some starting material (11%) was recovered after chromatographic purification (Method B).

192. ¹H-NMR (300 MHz, CDCl₃): δ 6.60-6.55 (m, 3H), 6.47, 5.82 (2bs, 1H), 6.04-5.97 (m, 2H), 5.81, 5.44 (2d, 1H), 5.05-5.00 (m, 1H), 4.95-4.93 (m, 1H), 4.67, 4.59 (2bs, 1H), 4.31 (s, 1H), 4.21 (s, 1H), 4.15-4.08 (m, 1H), 3.77, 3.76 (2s, 3H), 3.54 (s, 3H), 3.52-3.46 (m, 1H), 3.18-3.10 (m, 3H), 2.79-2.75 (m, 1H), 2.65-2.55 (m, 1H), 2.50-2.45 (m, 1H), 2.48 (t, 2H), 2.38-2.03 (m, 2H), 2.29 (s, 3H), 2.28, 2.27 (2s, 3H), 2.04, 1.96 (2s, 3H), 1.79-1.67 (m, 2H), 1.47, 1.32 (2s, 9H), 1.00 (t, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.3, 172.1, 171.6, 168.0, 154.6, 152.9, 148.5, 146.7, 145.9, 145.2, 143.2, 142.8, 141.4, 138.7, 132.3, 131.2, 130.7, 130.0, 129.8, 128.6, 122.5, 121.7, 121.3, 120.8, 120.5, 116.7, 116.4, 113.7, 113.4, 111.8, 101.9, 81.2, 80.9, 64.7, 61.2, 60.9, 60.3, 60.3, 60.1, 59.8, 58.4, 58.2, 57.9, 55.1, 48.5, 48.2, 47.3, 45.9, 42.3, 41.5, 39.6, 39.5, 35.8, 28.6, 28.3, 28.2, 28.1, 27.4, 20.6, 20.4, 18.5, 15.8, 13.5, 9.7, 9.6.

ESI-MS m/z: Calcd. for C₄₈H₅₄N₄O₁₃S: 926.3. Found (M+H⁺): 927.3.

EXAMPLE 170

Compound 193 is obtained using 10 equiv. of butyl chloride as the acid chloride and 10 equiv of Et₃N as base (Method B). Compound 192 (13%) is recovered after chromatographic purification.

193. ¹H-NMR (300 MHz, CDCl₃): δ 6.94 (s, 1H), 6.61 (s, 1H), 6.55 (s, 1H), 6.01 (d, 2H), 5.34-5.32 (m, 0.4H), 5.11-4.93 (m, 2.6H), 4.52-4.50 (m, 1H), 4.32-4.30 (m, 1H), 4.21 (d, 1H), 4.13-4.09 (m, 1H), 3.75, 3.74 (2s, 3H), 3.55 (s, 3H), 3.48-3.46 (m, 1H), 3.22-3.08 (m, 3H), 2.82-2.78 (m, 1H), 2.66-2.59 (m, 1H), 2.62 (t, 2H), 2.51-2.46 (m, 1H), 2.49 (t, 2H), 2.35-2.17 (m, 2H), 2.32, 2.31 (2s, 6H), 2.04 (s, 3H), 2.01-1.85 (m, 2H), 1.80-1.67 (m, 2H), 1.44, 1.37 (2s, 9H), 1.12 (t, 3H), 1.00 (t, 3H).

ESI-MS m/z: Calcd. for C₅₂H₆₀N₄O₁₄S: 996.4. Found (M+H⁺): 997.3.

EXAMPLE 171

Compound 194 is obtained using 2.5 equiv. of cinnamoyl chloride as the acid chloride and 3.5 equiv. of pyr as base (Method B). Compound 188 (8%) is recovered after chromatographic purification.

194 ¹H-NMR (300 MHz, CDCl₃): δ 7.80 (d, 1H), 7.68-7.54 (m, 2H), 7.50-7.38 (m, 3H), 6.69-6.57 (m, 4H), 6.47, 5.84 (2bs, 1H), 6.04-5.97 (m, 2H), 5.81, 5.45 (2d, 1H), 5.06-5.01 (m, 1H), 4.95-4.93 (m, 1H), 4.68, 4.61 (2bs, 1H), 4.32 (s, 1H), 4.23-4.10 (m, 2H), 3.77, 3.76 (2s, 3H), 3.57 (s, 3H), 3.52-3.47 (m, 1H), 3.19-3.09 (m, 3H), 2.82-2.78 (m, 1H), 2.69-2.62 (m, 1H), 2.54-2.47 (m, 1H), 2.41-2.20 (m, 2H), 2.30, 2.28 (2s, 6H), 2.04, 1.97 (2s, 3H), 1.47, 1.33 (2s, 9H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.3, 172.1, 168.1, 164.9, 152.9, 148.6, 146.7, 146.5, 145.9, 145.5, 143.2, 142.8, 138.6, 134.2, 132.3, 131.2, 130.7, 130.6, 130.3, 130.0, 129.8, 128.9, 128.7, 128.2, 128.1, 122.6, 121.3, 120.8, 120.5, 116.9, 116.7, 116.5, 113.7, 113.4, 111.8, 101.9, 81.2, 64.8, 61.2, 60.9, 60.3, 60.3, 60.2, 59.8, 58.4, 58.2, 57.9, 55.2, 48.5, 48.2, 47.3, 45.9, 42.3, 41.5, 39.6, 39.5, 28.6, 28.3, 28.2, 28.1, 27.4, 20.6, 20.4, 15.8, 9.7, 9.6.

ESI-MS m/z: Calcd. for C₅₃H₅₄N₄O₁₃S: 986.3. Found (M+H⁺): 987.3.

EXAMPLE 172

Method C: To a solution of 1 equiv. of starting material in CH₂Cl₂ (0.032M) under Argon were added 2 equiv. of acid, 2 equiv. of DMAP and 2 equiv. of EDC.HCl. The reaction was stirred at room temperature for 2 h. After this time was diluted with CH₂Cl₂, washed with brine and the organic layer dried over Na₂SO₄. Flash chromatography gives pure compounds.

Using 1.5 equiv. of octanoic acid as the acid, we obtain a mixture of compounds 195 and 196.

195: ¹H-NMR (300 MHz, CDCl₃): δ 6.59-6.55 (m, 3H), 6.08, 5.78 (bs, s, 1H), 6.04-5.97 (m, 2H), 5.72, 5.44 (2d, 1H), 5.05-4.99 (m, 1H), 4.95-4.92 (m, 1H), 4.65, 4.60 (2bs, 1H), 4.31, 4.30 (2s, 1H), 4.22-4.18 (m, 1H), 4.14-4.09 (m, 1H), 3.77 (1s, 3H), 3.54 (s, 3H), 3.47 (d, 1H), 3.18-3.06 (m, 3H), 2.79-2.75 (m, 1H), 2.65-2.55 (m, 1H), 2.52-2.44 (m, 1H), 2.49 (t, 2H), 2.37-2.14 (m, 2H), 2.30 (s, 3H), 2.28, 2.27 (2s, 3H), 2.04, 2.00 (2s, 3H), 1.74-1.64 (m, 2H), 1.46, 1.33 (2s, 9H), 1.37-1.28 (m, 8H), 0.87 (t, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.3, 172.1, 171.8, 168.1, 154.6, 152.9, 148.5, 146.6, 145.9, 145.5, 145.3, 143.1, 142.8, 141.4, 140.1, 139.9, 138.7, 132.3, 132.1, 131.2, 130.8, 129.9, 129.8, 128.7, 122.5, 121.7, 121.3, 120.7, 120.6, 116.6, 116.5, 114.7, 113.7, 113.4, 111.8, 102.0, 81.2, 80.9, 64.8, 61.2, 60.9, 60.4, 60.1, 59.9, 58.4, 58.2, 58.0, 55.1, 48.5, 48.2, 47.3, 45.9, 42.3, 41.6, 41.5, 39.6, 39.5, 34.0, 31.6, 28.9, 28.9, 28.6, 28.4, 28.2, 28.1, 27.4, 25.0, 22.6, 20.5, 20.4, 15.8, 14.0, 9.7.

ESI-MS m/z: Calcd. for C₅₂H₆₂N₄O₁₃S: 982.4. Found (M+H⁺): 983.3.

196: ¹H-NMR (300 MHz, CDCl₃): δ 6.94 (s, 1H), 6.60 (s, 1H), 6.55 (s, 1H), 6.01 (d, 2H), 5.34-5.30, 5.11-4.93 (2m, 3H), 4.52-4.49 (m, 1H), 4.34-4.32 (m, 1H), 4.22-4.09 (m, 2H), 3.74, 3.73 (2s, 3H), 3.55 (s, 3H), 3.48-3.45 (m, 1H), 3.22-3.07 (m, 3H), 2.82-2.79 (m, 1H), 2.65-2.60 (m, 1H), 2.62 (t, 2H), 2.52-2.45 (m, 1H), 2.50 (t, 2H), 2.37-2.17 (m, 2H), 2.31, 2.30 (2s, 6H), 2.04 (s, 3H), 1.89-1.82 (m, 2H), 1.75-1.65 (m, 2H), 1.59-1.23 (m, 16H), 1.44, 1.37 (2s, 9H), 0.90-0.85 (m, 6H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.2, 171.8, 170.1, 167.7, 153.1, 148.5, 147.8, 145.6, 141.3, 140.2, 138.8, 132.1, 131.9, 131.3, 128.8, 127.7, 126.6, 125.1, 122.5, 120.5, 116.2, 114.7, 113.7, 113.6, 111.7, 102.0, 81.5, 64.8, 61.2, 60.0, 59.9, 58.6, 58.4, 58.0, 55.1, 48.5, 47.8, 46.4, 42.5, 41.6, 39.6, 34.3, 34.0, 31.7, 29.3, 29.2, 28.9, 28.9, 28.6, 28.1, 28.0, 27.5, 25.2, 25.0, 22.6, 20.3, 15.9, 14.0, 9.7.

ESI-MS m/z: Calcd. for C₆₀H₇₆N₄O₁₄S: 1108.5. Found (M+H⁺): 1109.4.

EXAMPLE 173

Using 1.5 equiv. of palmitic acid as the acid, we obtain a mixture of compounds 197 and 198 (Method C).

197: ¹H-NMR (300 MHz, CDCl₃): δ 6.59-6.55 (m, 3H), 6.25, 5.78 (bs, s, 1H), 6.04-5.97 (m, 2H), 5.77, 5.44 (2bd, 1H), 5.05-5.00 (m, 1H), 4.96-4.93 (m, 1H), 4.66, 4.60 (2bs, 1H), 4.31 (bs, 1H), 4.23-4.19 (m, 1H), 4.15-4.09 (m, 1H), 3.77, 3.76 (2s, 3H), 3.54 (s, 3H), 3.50-3.47 (m, 1H), 3.18-3.07 (m, 3H), 2.79-2.75 (m, 1H), 2.66-2.57 (m, 1H), 2.52-2.47 (m, 1H), 2.49 (t, 2H), 2.39-2.13 (m, 2H), 2.30, 2.28, 2.27 (3s, 6H), 2.04, 1.98 (2s, 3H), 1.71-1.64 (m, 2H), 1.46, 1.33 (2s, 9H), 1.46-1.25 (m, 24H), 0.88 (t, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.3, 172.1, 171.8, 168.1, 154.6, 152.9, 148.5, 146.6, 145.9, 145.5, 143.1, 142.7, 141.4, 140.1, 138.7, 132.3, 131.2, 130.8, 129.8, 128.6, 122.5, 121.7, 121.3, 120.6, 116.6, 116.5, 113.7, 113.4, 111.8, 102.0, 81.2, 80.9, 64.8, 61.2, 60.9, 60.4, 60.1, 59.9, 58.4, 58.2, 58.0, 55.1, 53.4, 48.5, 48.2, 47.3, 45.9, 42.3, 41.6, 41.5, 39.6, 39.5, 34.0, 31.6, 29.7, 29.6, 29.6, 29.5, 29.3, 29.3, 29.0, 28.6, 28.2, 28.1, 27.4, 25.0, 22.7, 20.5, 20.4, 15.8, 14.1, 9.7.

ESI-MS m/z: Calcd. for C₆₀H₇₈N₄O₁₃S: 1094.5. Found (M+H⁺): 1095.4.

198: ¹H-NMR (300 MHz, CDCl₃): δ 6.94 (s, 1H), 6.60 (s, 1H), 6.54 (s, 1H), 6.01 (d, 2H), 5.34-5.33, 5.11-4.93 (2m, 3H), 4.53-4.52 (m, 1H), 4.32-4.29 (m, 1H), 4.22-4.09 (m, 2H), 3.74, 3.73 (2s, 3H), 3.55 (s, 3H), 3.48-3.46 (m, 1H), 3.22-3.09 (m, 3H), 2.82-2.78 (m, 1H), 2.65-2.60 (m, 1H), 2.62 (t, 2H), 2.52-2.47 (m, 1H), 2.50 (t, 2H), 2.37-2.17 (m, 2H), 2.31 (s, 3H), 2.30 (s, 3H), 2.04 (s, 3H), 1.89-1.81 (m, 2H), 1.72-1.64 (m, 2H), 1.44-1.25 (m, 48H), 1.44, 1.37 (2s, 9H), 0.90-0.85 (m, 6H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.1, 171.8, 170.4, 170.1, 167.7, 153.1, 148.5, 147.9, 145.6, 141.3, 140.2, 138.8, 132.1, 131.9, 131.3, 128.8, 127.7, 126.6, 125.1, 122.5, 120.5, 116.2, 114.7, 113.6, 111.7, 102.0, 81.5, 64.8, 61.2, 60.0, 58.6, 58.1, 55.1, 48.5, 47.8, 46.4, 42.5, 41.6, 39.6, 34.3, 34.0, 31.9, 29.7, 29.7, 29.5, 29.5, 29.3, 29.3, 29.0, 28.6, 28.1, 28.0, 27.4, 25.2, 25.0, 22.7, 20.3, 15.9, 14.1, 9.7.

ESI-MS m/z: Calcd. for C₇₆H₁₀₈N₄O₁₄S: 1332.8. Found (M+H⁺): 1333.6.

EXAMPLE 174

To a solution of 1 equiv. of compound 190 in DMF (0.02M) under Argon at room temperature, were added 0.7 equiv. of Cs₂CO₃ and 2 equiv. of allyl bromide. The reaction was stirred for 72 h and then quenched with AcOH. The crude was diluted with Hex/EtOAc 1:3, washed with a saturated solution of NaCl, the aqueous layers extracted with Hex/EtOAc 1:3, and the organic layers dried over Na₂SO₄. Flash cromatography gives pure compound 199 (66%).

199. ¹H-NMR (300 MHz, CDCl₃): δ 6.79 (s, 1H), 6.69 (s, 1H), 6.57, 6.56 (2s, 1H), 6.28-6.01 (m, 1H), 6.01 (d, 1H), 5.56-5.24 (m, 3H), 5.07-4.43 (m, 5H), 4.31-4.29 (m, 1H), 4.20-4.08 (m, 2H), 3.84, 3.81 (2s, 3H), 3.58 (s, 3H), 3.48-3.45 (m, 1H), 3.17-3.06 (m, 3H), 2.83-2.77 (m, 1H), 2.69-2.59 (m, 1H), 2.55-2.47 (m, 1H), 2.36-2.17 (m, 2H), 2.28 (s, 3H), 2.24 (s, 3H), 2.04 (s, 3H), 1.50, 1.43, 1.40 (3s, 18H).

ESI-MS m/z: Calcd. for C₅₂H₆₀N₄O₁₄S: 996.4. Found (M+H⁺): 997.2.

EXAMPLE 175

To a solution of compound 188 in CH₃CN (0.016M) at room temperature under Argon, were added 100 equiv. of formaline (37 wt. % in water) and 5 equiv. of NaCNBH₃. After 1 h 20 equiv. of acetic acid were added. The reaction mixture was stirred for 2 h more. After this time, it was diluted with CH₂Cl₂, neutralise with NaHCO₃ and extracted with CH₂Cl₂. The organic layers were dried over Na₂SO₄. Flash chromatography gives pure compound (86%).

200 ¹H-NMR (300 MHz, CDCl₃): δ 6.47-6.45 (m, 2H), 6.18 (s, 1H), 6.09-5.96 (m, 2H), 5.77, 5.42 (2s, 1H), 5.66, 5.43 (2d, 1H), 4.99-4.87 (m, 2H), 4.66, 4.62 (2bs, 1H), 4.35-4.32 (m, 1H), 4.13, 4.05 (2d, 1H), 3.90-3.83 (m, 1H), 3.77 (s, 3H), 3.55 (s, 3H), 3.49-3.44 (m, 1H), 3.23-3.13 (m, 2H), 3.04-2.93 (m, 1H), 2.71-2.56 (m, 3H), 2.47-2.17 (m, 2H), 2.32, 2.30 (2s, 3H), 2.2.20, 2.17 (2s, 6H), 2.02, 2.01 (2s, 3H), 1.46, 1.32 (2s, 9H).

ESI-MS m/z: Calcd. for C₄₅H₅₀N₄O₁₂S: 870.3. Found (M+H⁺): 871.2.

EXAMPLE 176

Method F: To a solution of 1 equiv. of starting material in CH₂Cl₂/H₂O/TFA 2:1:3.3 (0.013M) was stirred at room temperature for 15 min. The reaction was followed by TLC and neutralised with NaHCO₃, extracted with CH₂Cl₂ and the organic layers dried with Na₂SO₄. Flash chromatography gives pure compounds.

201 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.82 (s, 1H), 6.49 (s, 1H), 6.41 (bs, 1H), 6.16-5.98 (m, 1H), 6.03 (d, 2H), 5.46-5.23 (m, 2H), 5.03 (d, 1H), 4.86-4.79 (m, 1H), 4.56-3.81 (m, 7H), 3.63 (s, 3H), 3.55-3.52 (m, 1H), 3.49 (s, 3H), 3.14-2.96 (m, 3H), 2.86-2.17 (m, 8H), 2.25 (bs, 3H), 2.04 (1s, 3H).

ESI-MS m/z: Calcd. for C₄₂H₄₄N₄O₁₀S: 796.3. Found (M+H⁺): 797.3.

EXAMPLE 177

202 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.62 (s, 1H), 6.61 (s, 1H), 6.56 (s, 1H), 6.00 (dd, 2H), 5.78 (bs, 1H), 5.02 (d, 1H), 4.56 (bs, 1H), 4.50 (d, 1H), 4.34 (s, 1H), 4.19 (d 1H), 4.11 (dd, 1H), 3.86-3.83 (m, 1H), 3.78 (s, 3H), 3.56 (s, 3H), 3.53 (bd, 1H), 3.14-3.09 (m, 2H), 2.99 (dd, 1H), 2.83-2.73 (m, 1H), 2.68-2.59 (m, 1H), 2.51-2.45 (m, 1H), 2.38-2.17 (m, 2H), 2.31 (s, 3H), 2.27 (s, 3H), 2.24 (s, 3H), 2.03 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.0, 169.0, 168.2, 148.4, 145.7, 145.4, 142.7, 141.3, 140.1, 138.5, 132.4, 131.3, 129.5, 128.6, 124.3, 122.5, 121.3, 120.9, 118.1, 113.9, 111.7, 101.9, 64.8, 61.2, 60.4, 60.0, 59.0, 58.8, 55.1, 48.6, 47.6, 41.9, 39.6, 28.6, 28.1, 20.6, 20.4, 15.8, 9.7.

ESI-MS m/z: Calcd. for C₄₁H₄₂N₄O₁₁S: 798.3. Found (M+H⁺): 799.3.

EXAMPLE 178

203 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.62 (s, 1H), 6.60 (s, 1H), 6.57 (s, 1H), 5.97 (dd, 2H), 5.78 (bs, 1H), 5.02 (d, 1H), 4.56 (bs, 1H), 4.50 (d, 1H), 4.34 (s, 1H), 4.19 (d 1H), 4.10 (dd, 1H), 3.86-3.83 (m, 1H), 3.78 (s, 3H), 3.55 (s, 3H), 3.53 (bd, 1H), 3.14-3.09 (m, 2H), 2.99 (dd, 1H), 2.82-2.75 (m, 1H), 2.63-2.55 (m, 1H), 2.52-2.46 (m, 1H), 2.48 (t, 2H), 2.38-2.17 (m, 2H), 2.31 (s, 3H), 2.27 (s, 3H), 2.03 (s, 3H), 1.79-1.67 (m, 2H), 1.00 (t, 3H).

ESI-MS m/z: Calcd. for C₄₃H₄₆N₄O₁₁S: 826.3. Found (M+H⁺): 827.3.

EXAMPLE 179

204 was obtained using Method F ¹H-NMR (300 MHz, CDCl₃): δ 7.81 (d, 1H), 7.58-7.54 (m, 2H), 7.41-7.39 (m, 3H), 6.66 (d, 1H), 6.63 (s, 1H), 6.60 (s, 1H), 6.57 (s, 1H), 6.01 (d, 2H), 5.79 (bs, 1H), 5.04 (d, 1H), 4.57 (bs, 1H), 4.51 (d, 1H), 4.34 (s, 1H), 4.20 (d 1H), 4.12 (dd, 1H), 3.87-3.84 (m, 1H), 3.79 (s, 3H), 3.57 (s, 3H), 3.54 (bd, 1H), 3.15-3.09 (m, 2H), 3.00 (dd, 1H), 2.83-2.78 (m, 1H), 2.75-2.62 (m, 1H), 2.54-2.48 (m, 1H), 2.41-2.19 (m, 2H), 2.32 (s, 3H), 2.28 (s, 3H), 2.03 (s, 3H).

¹³C-NMR (300 MHz, CDCl₃): δ 172.2, 168.2, 164.9, 148.6, 146.5, 145.8, 145.4, 142.8, 141.4, 140.1, 138.6, 134.2, 132.5, 131.3, 130.6, 129.6, 128.9, 128.7, 128.3, 124.4, 122.6, 121.0, 118.1, 116.9, 113.9, 113.4, 111.8, 101.9, 64.9, 61.2, 60.4, 60.0, 59.1, 58.8, 55.2, 48.6, 47.6, 42.2, 42.0, 39.6, 28.7, 28.2, 20.4, 15.8, 9.7.

ESI-MS m/z: Calcd. for C₄₈H₄₆N₄O₁₁S: 886.3. Found (M+H⁺): 887.2.

EXAMPLE 180

205 was obtained using Method F ¹H-NMR (300 MHz, CDCl₃): δ 6.62 (s, 1H), 6.60 (s, 1H), 6.56 (s, 1H), 6.02 (d, 2H), 5.79 (bs, 1H), 5.03 (d, 1H), 4.57 (bs, 1H), 4.51 (d, 1H), 4.34 (s, 1H), 4.20 (d 1H), 4.12 (dd, 1H), 3.87-3.84 (m, 1H), 3.79 (s, 3H), 3.55 (s, 3H), 3.54 (bd, 1H), 3.15-3.09 (m, 2H), 3.00 (dd, 1H), 2.82-2.78 (m, 1H), 2.68-2.60 (m, 1H), 2.53-2.46 (m, 1H), 2.50 (t, 2H), 2.39-2.18 (m, 2H), 2.32 (s, 3H), 2.28 (s, 3H), 2.04 (s, 3H), 1.73-1.65 (m, 2H), 1.39-1.24 (m, 8H), 0.88 (t, 3H).

ESI-MS m/z: Calcd. for C₄₇H₅₄N₄O₁₁S: 882.3. Found (M+H⁺): 883.3.

EXAMPLE 181

206 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.95 (s, 1H), 6.60 (s, 1H), 6.53 (s, 1H), 6.02 (dd, 2H), 5.02 (d, 1H), 4.45 (bs, 1H), 4.35 (s, 1H), 4.20 (d, 1H), 4.11 (dd, 1H), 4.04 (d, 1H), 3.88-3.85 (m, 1H), 3.74 (s, 3H), 3.54 (bs, 4H), 3.17-3.08 (m, 2H), 3.01 (dd, 1H), 2.83-2.78 (m, 1H), 2.64-2.59 (m, 1H), 2.62 (t, 2H), 2.52-2.47 (m, 1H), 2.50 (t, 2H), 2.38-2.17 (m, 2H), 2.31 (s, 3H), 2.29 (s, 3H), 2.04 (s, 3H), 1.87-1.77 (m, 2H), 1.72-1.64 (m, 2H), 1.49-1.23 (m, 16H), 0.89-0.85 (m, 6H).

ESI-MS m/z: Calcd. for C₅₅H₆₈N₄O₁₂S: 1008.5. Found (M+H⁺): 1009.4.

EXAMPLE 182

207 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.62 (s, 1H), 6.59 (s, 1H), 6.55 (s, 1H), 6.01 (dd, 2H), 5.78 (bs, 1H), 5.02 (d, 1H), 4.56 (bs, 1H), 4.50 (d, 1H), 4.33 (s, 1H), 4.19 (d 1H), 4.10 (dd, 1H), 3.86-3.83 (m, 1H), 3.78 (s, 3H), 3.54 (s, 3H), 3.53 (bd, 1H), 3.14-3.08 (m, 2H), 2.99 (dd, 1H), 2.81-2.78 (m, 1H), 2.68-2.55 (m, 1H), 2.52-2.45 (m, 1H), 2.49 (t, 2H), 2.38-2.17 (m, 2H), 2.31 (s, 3H), 2.27 (s, 3H), 2.03 (s, 3H), 1.72-1.64 (m, 2H), 1.38-1.25 (m, 24H), 0.87 (t, 3H).

ESI-MS m/z: Calcd. for C₅₅H₇₀N₄O₁₁S: 994.5. Found (M+H⁺): 995.5.

EXAMPLE 183

208 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.96 (s, 1H), 6.60 (s, 1H), 6.53 (s, 1H), 6.02 (dd, 2H), 5.02 (d, 1H), 4.45 (bs, 1H), 4.35 (s, 1H), 4.20 (d, 1H), 4.10 (dd, 1H), 4.05 (d, 1H), 3.88-3.85 (m, 1H), 3.74 (s, 3H), 3.55 (bs, 4H), 3.17-3.07 (m, 2H), 3.01 (dd, 1H), 2.84-2.80 (m, 1H), 2.69-2.59 (m, 1H), 2.62 (t, 2H), 2.52-2.47 (m, 1H), 2.50 (t, 2H), 2.37-2.19 (m, 2H), 2.32 (s, 3H), 2.29 (s, 3H), 2.04 (s, 3H), 1.87-1.77 (m, 2H), 1.74-1.64 (m, 2H), 1.45-1.25 (m, 48H), 0.88 (t, 6H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.1, 171.9, 171.3, 167.6, 148.4, 147.6, 145.6, 141.4, 141.3, 140.2, 138.7, 132.1, 131.6, 131.3, 130.1, 128.6, 128.0, 122.5, 120.7, 117.8, 113.8, 111.7, 102.0, 72.5, 65.0, 64.9, 61.2, 60.2, 59.9, 58.9, 58.4, 55.1, 48.7, 48.4, 42.3, 42.2, 39.6, 34.2, 34.0, 31.9, 29.7, 29.6, 29.5, 29.3, 29.2, 29.0, 28.6, 27.7, 25.2, 25.0, 22.7, 20.3, 15.8, 14.1, 9.7.

ESI-MS m/z: Calcd. for C₇₁H₁₀₀N₄O₁₂S: 1232.7. Found (M+H⁺): 1233.6.

EXAMPLE 184

209 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.50 (s, 1H), 6.44 (s, 1H), 6.19 (s, 1H), 6.02 (d, 2H), 5.77 (bp 1H), 5.46 (bp, 1H), 4.96 (d, 1H), 4.59 (bp, 1H), 4.50 (d, 1H), 4.35 (s, 1H), 4.10 (d, 1H), 3.87-3.82 (m, 2H), 3.78 (s, 3H), 3.54 (s, 3H), 3.53 (d, 1H), 3.30-3.15 (m, 1H), 3.07-2.91 (m, 2H), 2.69-2.55 (m, 3H), 2.46-2.39 (m, 2H), 2.30 (s, 3H), 2.23 (s, 3H), 2.19 (s, 3H), 2.02 (s, 3H).

ESI-MS m/z: Calcd. for C₄₀H₄₂N₄O₁₀S: 770.3. Found (M+H⁺): 771.3.

EXAMPLE 185

Method H: To a solution of 1 equiv. of starting material in CH₃CN/H₂O 3:2 (0.009M) were added 30 equiv. of AgNO₃. After 24 h the reaction was quenched with a mixture 1:1 of saturated solutions of brine and NaHCO₃, stirred for 10 min and diluted and extracted with CH₂Cl₂. The organic layer was dried over Na₂SO₄. Chromatography gives pure compounds.

210 was obtained using Method H. ¹H-NMR (300 MHz, CDCl₃): δ 6.62 (s, 1H), 6.60 (s, 1H), 6.56 (s, 1H), 5.99, 5.97 (2d, 2H), 5.13 (d, 1H), 4.84, 4.74 (2s, 1H), 4.52 (d, 1H), 4.45 (bs, 1H), 4.38 (d 1H), 4.02 (dd, 1H), 3.78 (s, 3H), 3.64-3.54 (m, 2H), 3.54 (s, 3H), 3.17-3.00 (m, 2H), 2.92-2.80 (m, 2H), 2.69-2.46 (m, 2H), 2.40-2.17 (m, 2H), 2.31 (s, 3H), 2.27 (s, 3H), 2.24 (s, 3H), 2.02 (s, 3H).

ESI-MS m/z: Calcd. for C₄₀H₄₃N₃O₁₂S: 789.3. Found (M−H₂O+H⁺): 772.3.

EXAMPLE 186

211 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.62 (s, 1H), 6.59 (s, 1H), 6.56 (s, 1H), 5.99, 5.98 (d, dd, 2H), 5.76 (bp, 1H), 5.14 (d, 1H), 4.84, 4.74 (2s, 1H), 4.52-4.37 (m, 3H), 1.06-4.00 (m, 1H), 3.78 (s, 3H), 3.67-3.54 (m, 2H), 3.54 (s, 3H), 3.12-3.00 (m, 2H), 2.92-2.80 (m, 2H), 2.68-2.60 (m, 1H), 2.51-2.46 (m, 1H), 2.48 (t, 2H), 2.40-1.99 (m, 2H), 2.31 (s, 3H), 2.27 (s, 3H), 2.02 (s, 3H), 1.80-1.67 (m, 2H), 1.00 (t, 3H).

ESI-MS m/z: Calcd. for C₄₂H₄₇N₃O₁₂S: 817.3. Found (M−H₂O+H⁺): 800.2.

EXAMPLE 187

212 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 7.81 (d, 1H), 7.57-7.54 (m, 2H), 7.41-7.39 (m, 3H), 6.66 (d, 1H), 6.63 (s, 1H), 6.60 (s, 1H), 6.58 (s, 1H), 5.99, 5.98 (2d, 2H), 5.75 (bp, 1H), 5.15 (d, 1H), 4.85, 4.75 (2s, 1H), 4.54-4.38 (m, 3H), 4.06-4.03 (m, 1H), 3.79 (s, 3H), 3.65-3.56 (m, 2H), 3.56 (s, 3H), 3.18-3.02 (m, 2H), 2.93-2.80 (m, 2H), 2.66-2.62 (m, 1H), 2.54-2.49 (m, 1H), 2.42-2.20 (m, 2H), 2.32 (s, 3H), 2.28 (s, 3H), 2.02 (s, 3H).

ESI-MS m/z: Calcd. for C₄₇H₄₇N₃O₁₂S: 877.3. Found (M−H₂O+H⁺): 860.3.

EXAMPLE 188

213 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.62 (s, 1H), 6.59 (s, 1H), 6.56 (s, 1H), 5.99, 5.98 (2d, 2H), 5.72 (bs, 1H), 5.14 (d, 1H), 4.84, 4.74 (2s, 1H), 4.51-4.37 (m, 3H), 4.06-4.04 (m, 1H), 7.78, 3.76 (2s, 3H), 3.64-3.54 (m, 2H), 3.54, 3.53 (2s, 3H), 3.15-3.00 (m, 2H), 2.92-2.83 (m, 2H), 2.68-2.47 (m, 2H), 2.49 (t, 2H), 2.40-2.27 (m, 2H), 2.31 (s, 3H), 2.27 (s, 3H), 2.02 (s, 3H), 1.72-1.65 (m, 2H), 1.39-1.24 (m, 8H), 0.88 (t, 3H).

ESI-MS m/z: Calcd. for C₄₆H₅₅N₃O₁₂S: 873.4. Found (M−H₂O+H⁺): 856.3.

EXAMPLE 189

214 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.96 (s, 1H), 6.60 (s, 1H), 6.54 (s, 1H), 5.99 (d, 2H), 5.14 (d, 1H), 4.84, 4.77 (2s, 1H), 4.54 (bp, 1H), 4.36 (bp, 1H), 4.02 (dd, 1H), 3.90 (d, 1H), 3.75 (s, 3H), 3.62-3.49 (m, 2H), 3.54 (s, 3H), 3.15-2.86 (m, 4H), 2.64-2.47 (m, 2H), 2.62 (t, 2H), 2.50 (t, 2H), 2.41-2.17 (m, 2H), 2.32 (s, 3H), 2.29 (s, 3H), 2.03 (s, 3H), 1.85-1.67 (m, 4H), 1.50-1.25 (m, 16H), 0.90-0.85 (m, 6H).

ESI-MS m/z: Calcd. for C₅₄H₆₉N₃O₁₃S: 999.5. Found (M−H₂O+H⁺): 982.4.

EXAMPLE 190

215 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.62 (s, 1H), 6.59 (s, 1H), 6.55 (s, 1H), 5.99, 5.98 (2d, 2H), 5.13 (d, 1H), 4.84, 4.74 (2s, 1H), 4.52 (d, 1H), 4.45 (bs, 1H), 4.38 (d 1H), 4.02 (dd, 1H), 3.78 (s, 3H), 3.76-3.53 (m, 2H), 3.53 (s, 3H), 3.16-3.00 (m, 2H), 292-2.80 (m, 2H), 2.63-2.58 (m, 1H), 2.52-2.47 (m, 3H), 2.40-2.19 (m, 2H), 2.31 (s, 3H), 2.27 (s, 3H), 2.02 (s, 3H), 1.72-1.67 (m, 2H), 1.38-1.25 (m, 24H), 0.87 (t, 3H).

ESI-MS m/z: Calcd. for C₅₄H₇₁N₃O₁₂S: 986.2. Found (M−H₂O⁺): 968.5.

EXAMPLE 191

216 was obtained using Method F. ¹H-NMR (300 MHz, CDCl₃): δ 6.96 (s, 1H), 6.60 (s, 1H), 6.54 (s, 1H), 6.00, 5.99 (d, dd, 2H), 5.14 (d, 1H), 4.85, 4.78 (2s, 1H), 4.54 (bp, 1H), 4.35 (bp, 1H), 4.02 (dd, 1H), 3.90 (d, 1H), 3.75 (s, 3H), 3.62-3.49 (m, 2H), 3.54 (s, 3H), 3.17-2.86 (m, 4H), 2.70-2.59 (m, 3H), 2.52-2.47 (m, 3H), 2.40-2.17 (m, 2H), 2.32 (s, 3H), 2.29 (s, 3H), 2.03 (s, 3H), 1.85-1.67 (m, 4H), 1.45-1.25 (m, 48H), 0.88 (t, 6H).

ESI-MS m/z: Calcd. for C₇₀H₁₀₁N₃O₁₃S: 1224.6. Found (M−H₂O⁺): 1206.6.

EXAMPLE 192

217 was obtained using Method F. ¹H-NMR (300 MHz, CD₃OD): δ 6.43 (s, 1H), 6.36 (s, 1H), 6.20 (s, 1H), 6.06 (d, 2H), 5.04 (d, 1H), 4.75 (d, 1H), 4.60 (bp, 1H), 4.42 (d 1H), 4.10 (d, 1H), 3.81 (dd, 1H), 3.72 (s, 3H), 3.65-3.60 (m, 2H), 3.51 (s, 3H), 3.13-3.01 (m, 2H), 2.86 (d, 1H), 2.65-2.32 (m, 5H), 2.32 (s, 3H), 2.21 (s, 3H), 2.19 (s, 3H), 2.01 (s, 3H).

ESI-MS m/z: Calcd. for C₃₉H₄₃N₃O₁₁S: 761.3 Found (M+H⁺): 762.3.

EXAMPLE 193

A solution of N-methylpyridine-4-carboxaldehyde iodide in anhydrous DMF (0.26M) was treated with anhydrous toluene (2×5 mL). A solution of compound 218 (118.7 mg, 1 equiv) (previously treated with anhydrous toluene 2×5 mL) in anhydrous CH₂Cl₂ (0.03M) was added, via cannula, at 23° C. to the solution of N-methylpyridine-4-carboxaldehyde iodide. The reaction mixture was stirred at 23° C. for 4 hours. After this time DBU (1.0 equiv) was dropwise added at 23° C. and was stirred for 15 minutes at 23° C. A freshly aqueous saturated solution of oxalic acid (5.4 mL) was added to the reaction mixture and was stirred for 30 minutes at 23° C. Then the reaction mixture was cooled to 0° C. and NaHCO₃ was portionwise added followed by addition of aqueous saturated solution of NaHCO₃. The mixture was extracted with Et₂O. The combined organic layers were dried over Na₂SO₄, filtered and the solvent was removed under reduced pressure. Flash chromatography gives pure compound 219 (54%).

219. ¹H-NMR (300 MHz, CDCl₃): δ 6.46 (s, 1H), 6.06 (dd, 2H), 5.59 (s, 1H), 5.08 (d, 1H), 4.66 (bs, 1H), 4.54 (bs, 1H), 4.38 (s, 1H), 4.28 (dd, 1H), 4.20 (dd, 1H), 4.14 (d, 1H), 3.54 (d, 1H), 3.43-3.40 (m, 1H), 2.93-2.82 (m, 2H), 2.71-2.55 (m, 2H), 2.34 (s, 3H), 2.19 (s, 3H), 2.13 (s, 3H), 2.04 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 186.5, 168.7, 160.5, 146.4, 143.5, 141.6, 140.6, 138.2, 127.2, 123.3, 121.0, 120.0, 118.0, 117.5, 113.4, 113.3, 102.2, 61.8, 61.3, 59.8, 59.0, 54.6, 54.5, 43.1, 41.6, 36.9, 23.9, 20.4, 15.7, 9.7.

ESI-MS m/z: Calcd. for C₃₀H₂₉N₃O₉S: 607.3 Found (M+H⁺): 608.2.

EXAMPLE 194

To a solution of 1 equiv. of compound 219 in EtOH (0.03M) were added 5 equiv. of AcOH and 3.5 equiv. of 2-[3-hydroxy-4-methoxyphenyl]ethylamine. The reaction was stirred overnight. Then the solvent was eliminated under reduced pressure. Flash chromatography gives pure compound (62%).

220. ¹H-NMR (300 MHz, CDCl₃): δ 6.54 (s, 1H), 6.44 (s, 1H), 6.41 (s, 1H), 6.01 (d, 2H), 4.98 (d, 1H), 4.58-4.40 (bm, 4H), 4.29 (s, 1H), 4.26 (d, 1H), 4.13-4.09 (m, 2H), 3.61 (s, 3H), 3.51-3.49 (m, 1H), 3.41-3.38 (m, 1H), 3.21 (dt, 1H), 3.00-2.85 (m, 3H), 2.71-2.60 (m, 1H), 2.42-1.97 (m, 3H), 2.28 (s, 6H), 2.21 (s, 3H), 2.04 (s, 3H).

¹³C-NMR (75 MHz, CDCl₃): δ 172.1, 145.6, 145.3, 144.7, 144.5, 141.4, 140.0, 138.5, 128.7, 127.8, 124.9, 120.8, 119.8, 118.1, 118.0, 114.0, 113.8, 109.8, 101.8, 64.3, 60.9, 60.6, 60.2, 59.6, 55.2, 54.9, 54.6, 42.2, 41.7, 41.6, 28.3, 24.2, 20.5, 15.9, 9.7.???

ESI-MS m/z: Calcd. for C₃₉H₄₀N₄O₁₀S: 756.3 Found (M+H⁺): 757.2.

EXAMPLE 195

To a solution of 1 equiv. of compound 220 in CH₃CN/H₂O 3:2 (0.015M) were added 30 equiv. of AgNO₃. The reaction was stirred for 24 h protected from the light. After this time, 2 mL of a saturated solution of NaCl and 2 mL of a saturated solution of NaHCO₃ were added and the crude was stirred for 10 min. Then it was diluted with CH₂Cl₂, washed with 15 mL of brine and extracted with CH₂Cl₂. The organic layer was dried over Na₂SO₄, filtered and the solvent was eliminated under reduced pressure. Preparative chromatography gives pure compound (11%).

221 ¹H-NMR (300 MHz, CDCl₃): δ 6.57 (s, 1H), 6.49 (s, 1H), 6.44 (s, 1H), 5.99 (d, 2H), 5.10 (d, 1H), 4.80 (s, 1H), 4.50-4.46 (m, 2H), 4.16 (d, 1H), 4.07 (m, 1H), 3.62 (s, 3H), 3.58-3.57 (m, 1H), 3.23-3.19 (m, 1H), 3.00-2.83 (m, 3H), 2.71-2.60 (m, 1H), 2.48-1.97 (m, 4H), 2.32 (s, 3H), 2.29 (s, 3H), 2.20 (s, 3H), 2.03 (s, 3H).

ESI-MS m/z: Calcd. for C₃₈H₄₁N₃O₁₁S: 747.3 Found (M−H₂O+H⁺): 730.2.

EXAMPLE 196

To a solution of 1 equiv. of compound 222 in EtOH (0.064M) under Argon at room temperature were added 3.5 equiv. of a-ethyl-3-hydroxy-4-methylphenethylamine chlorhydrate and 2 equiv. of K₂CO₃ and silica gel. The reaction was stirred at room temperature for 7 hours. Then the solvent was eliminated under reduced pressure. Flash chromatography gives pure compound (68%). Compound 223 is isolated as a mixture of two isomers. These compounds can also be obtained when the reaction is performed with acetic acid as solvent and heating at 50° C. for 24 hours (99%).

223. ¹H-NMR (300 MHz, CDCl₃): δ 6.79 (s, 1H), 6.57 (s, 1H), 6.54 (s, 1H), 6.51 (s, 1H), 6.19 (s, 1H), 6.13-6.08 (m, 3H), 6.03-6.02 (m, 2H), 5.74 (s, 1H), 5.71 (d, 1H); 5.03 (d, 1H); 4.94 (d, 1H), 4.56 (s, 2H), 4.34-4.08 (m, 10H); 3.77 (s, 3H), 3.76 (s, 3H), 3.51-3-49 (m, 2H), 3.41 (s, 2H), 2.96-2.87 (m, 4H), 2.51-2.37 (m, 2H), 2.29 (s, 3H), 2.28 (s, 3H), 2.26 (s, 3H), 2.24 (s, 3H), 2.15 (s, 3H), 2.09 (s, 3H), 2.06 (s, 3H), 2.04 (s, 3H), 2.00 (s, 3H), 1.47-1.34 (m, 4H); 0.98 (t, 6H).

ESI-MS m/z: Calcd. for C₄₂H₄₆N₄O₉S: 782.3 Found (M+H⁺): 783.3.

EXAMPLE 197

To a solution of 1 equiv. of compound 223 in CH₃CN/H₂O 3:2 (0.01M) were added 30 equiv. of AgNO₃. The reaction was stirred at room temperature for 24 h protected from the light. After this time, the reaction was quenched with a mixture 1:1 of an aqueous saturated solutions of NaCl and NaHCO₃, stirred for 10 min and diluted and extracted with CH₂Cl₂. The organic layer was dried over Na₂SO₄, filtered and the solvent was eliminated under reduced pressure. Chromatography gives a mixture of the two isomers compound 224 (72%).

224A First isomer: ¹H-NMR (300 MHz, CDCl₃): δ 6.59(s, 1H); 6.52 (s, 1H); 6.29 (s, 1H); 6.06 (d, 1H); 6.01 (d, 1H); 5.68 (s, 1H); 5.06 (d, 1H); 4.80 (s, 1H); 4.48 (m, 2H); 4.16 (d, 1H); 4.07 (dd, 1H); 3.78 (s, 3H); 3.59 (d, 3H); 3.23-3.21 (m, 1H); 3.05-3.01 (m, 1H); 2.87-2.84 (m, 2H); 2.44-2.20 (m, 2H); 2.28 (s, 3H); 2.25 (s, 3H); 2.14 (s, 3H); 2.06 (s, 3H), 2.01 (s, 3H), 1.45 (m, 2H), 1.01 (t, 3H).

ESI-MS m/z: Calcd. for C₄₁H₄₇N₃O₁₀S: 773.3 Found (M−H₂O+H⁺): 756.2.

224B Second isomer: ¹H-NMR (300 MHz, CDCl₃): δ 6.80(s, 1H); 6.55 (s, 1H); 6.26 (s, 1H); 6.09 (d, 1H); 6.00 (d, 1H); 5.66 (s, 1H); 5.12 (d, 1H); 4.82 (s, 1H); 4.48 (m, 2H); 4.20-4.13 (m, 3H); 3.77 (s, 3H); 3.57 (d, 1H); 3.21 (s, 1H); 2.83-2.80 (m, 2H); 2.55-2.50 (m, 1H); 2.33-2.06 (m, 2H), 2.30 (s, 3H); 2.27 (s, 3H); 2.08 (s, 3H), 2.03 (s, 6H), 1.45-1.37 (m, 2H), 1.01 (t, 3H).

ESI-MS m/z: Calcd. for C₄₁H₄₇N₃O₁₀S: 773.3 Found (M−H₂O+H⁺): 756.3.

Bioassays for Antitumor Screening

The finality of these assays is to interrupt the growth of a “in vitro” tumor cell culture by means a continued exhibition of the cells to the sample to be testing.

CELL LINES Tissue Name N^(o) ATCC Species ascites Characteristics P-388 CCL-46 mouse fluid lymphoid neoplasm K-562 CCL-243 human leukemia erythroleukemia (pleural effusion) A-549 CCL-185 human lung lung carcinoma “NSCL” SK-MEL-28 HTB-72 human melanoma malignant melanoma HT-29 HTB-38 human colon colon adenocarcinoma LoVo CCL-229 human colon colon adenocarcinoma LoVo-Dox human colon colon adenocarcinoma (MDR) SW620 CCL-228 human colon colon adenocarcinoma (lymph node metastasis) DU-145 HTB-81 human prostate prostate carcinoma, not androgen receptors LNCaP CRL-1740 human prostate prostate adenocarcinoma, with androgen receptors SK-BR-3 HTB-30 human breast breast adenocarcinoma, Her2/neu+, (pleural effusion) MCF-7 HTB-22 human breast breast adenocarcinoma, (pleural effusion) MDA-MB-231 HTB-26 human breast breast adenocarcinoma, Her2/neu+, (pleural effusion) IGROV-1 human ovary ovary adenocarcinoma IGROV-ET human ovary ovary adenocarcinoma, characterized as ET-743 resistant cells SK-OV-3 HTB-77 human ovary ovary adenocarcinoma (malignant ascites) OVCAR-3 HTB-161 human ovary ovary adenocarcinoma HeLa CCL-2 human cervix cervix epitheloid carcinoma HeLa-APL CCL-3 human cervix cervix epitheloid carcinoma, characterized as aplidine resistant cells A-498 HTB-44 human kidney kidney carcinoma PANC-1 CRL-1469 human pancreas pancreatic epitheloid carcinoma HMEC1 human endothelium 1°.—Inhibition of Cell Growth by Counting Cells.

This form of the assay employs 24 well multidishes of 16 mm diameter (Bergeron, 1984; Schroeder, 1981). The tumor cell lines employed are: P-388 (ATCC CCL 46), suspension culture of a lymphoid neoplasm from a DBA/2 mouse; A-549 (ATCC CCL 185), monolayer culture of a human lung carcinoma; HT-29 (ATCC HTB-38), monolayer culture of a human colon carcinoma; MEL-28 (ATCC HTB-72), monolayer culture of a human melanoma and DU-145 (ATCC HTB-81), monolayer culture of a human prostate carcinoma.

Cells were maintained, in logarithmic phase of growth in Eagle's Minimum Essential Medium, with Earle's Balanced Salts, with non-essential amino acids, with 2.0 mM L-Glutamine, without sodium bicarbonate (EMEM/neaa), supplemented with 10% Fetal Calf Serum (FCS), 10⁻² M. sodium bicarbonate and 0.1 U/l penicillin G+0.1 g/l streptomycin sulfate. For the experiments, cells are harvested from subconfluent cultures using trypsin and resuspended in fresh medium before plating.

P-388 cells were seeded into 16 mm diameter wells at 1×10⁴ cells per well in 1 ml aliquots of EMEM 5% FCS containing different concentrations of the sample to be tested. A separate set of cultures without drug was seeded as control of growth, to ensure that cells remained in exponential phase of growth. All determinations are carrying out in duplicate. After three days of incubation at 37° C., 5% CO₂ in a 98% humid atmosphere, an approximately IC50 was determined by comparing the growth in wells with drug to the growth in wells control.

A-549, HT-29, MEL-28 and DU-145 cells were seeded into 16 mm diameter wells at 1×10⁴ cells per well in 1 ml aliquots of EMEM 5% FCS containing different concentrations of the sample to be tested. A separate set of cultures without drug was seeded as control of growth, to ensure that cells remained in exponential phase of growth. All determinations are carrying out in duplicate. After three days of incubation at 37° C., 5% CO₂ in a 98% humid atmosphere cells were stained with 0.1% crystal violet. An approximately IC50 was determined by comparing the growth in wells with drug to the growth in wells control.

For quantifying the activity, after the incubation time, cells are trypsinized and counted in a Coulter Counter ZM. All counts (net cells per well), represent the average of duplicate wells. % G, percent of growth relative to cultures without drug. The results of these assays are used to generate dose-response curves from which more precise IC50 values are determined (sample concentration which produces 50% cell growth inhibition).

Obtained results may predict the usefulness of a certain drug as a potential cancer treatment. For this technique, compounds which show IC50 values smaller than 1 μg/ml are selected to continue with further studies. IC50's data allow to predict that not only could a drug be cystostatic, but also it could have a potential in terms of tumor reduction.

2°.—Inhibition of Cells Growth by Colorimetric Assay.

A colorimetric type of assay, using sulforhodamine B (SRB) reaction has been adapted for a quantitative measurement of cell growth and viability [following the technique described by Philip Skehan, et al. (1990), New colorimetric cytotoxicity assay for anticancer drug screening, J. Natl. Cancer Inst., 82:1107-1112]

This form of the assay employs 96 well cell culture microplates of 9 mm diameter (Faircloth, 1988; Mosmann, 1983). Most of the cell lines are obtained from American Type Culture Collection (ATCC) derived from different human cancer types.

Cells are maintained in RPMI 1640 10% FBS, supplemented with 0.1 g/l penicillin and 0.1 g/l streptomycin sulfate and then incubated at 37° C., 5% CO₂ and 98% humidity. For the experiments, cells were harvested from subconfluent cultures using trypsin and resuspended in fresh medium before plating.

Cells are seeded in 96 well microtiter plates, at 5×10³ cells per well in aliquots of 195 μl medium, and they are allowed to attach to the plate surface by growing in drug free medium for 18 hours. Afterward, samples are added in aliquots of 5 μl in a ranging from 10 to 10⁻⁸ μg/ml, dissolved in DMSO/EtOH/PBS (0.5:0.5:99). After 48 hours exposure, the antitumor effect are measured by the SRB methodology: cells are fixed by adding 50 μl of cold 50% (wt/vol) trichloroacetic acid (TCA) and incubating for 60 minutes at 4° C. Plates are washed with deionized water and dried. One hundred μl of SRB solution (0.4% wt/vol in 1% acetic acid) is added to each microtiter well and incubated for 10 minutes at room temperature. Unbound SRB is removed by washing with 1% acetic acid. Plates are air dried and bound stain is solubilized with Tris buffer. Optical densities are read on a automated spectrophotometric plate reader at a single wavelength of 490 nm.

The values for mean+/−SD of data from triplicate wells are calculated. Some parameters for cellular responses can be calculated: GI=growth inhibition, TGI=total growth inhibition (cytostatic effect) and LC=cell killing (cytotoxic effect).

Obtained results may predict the usefulness of a certain drug as a potential cancer treatment. For this technique, compounds which show GI50 values smaller than 10 μg/ml are selected to continue with further studies. GI50's data allow to predict that not only could a drug be cystostatic, but also it could have a potential in terms of tumor reduction.

Activity Data IC₅₀ (molar) Compound P-388 A-549 HT-29 MEL-28 DU-145 2 1.48E-10 1.48E-10 1.48E-10 1.48E-10 3 1.15E-09 1.15E-09 1.15E-09 1.15E-09 1.15E-09 4 1.15E-10 1.15E-10 1.15E-10 1.15E-10 1.15E-10 5 5.15E-10 5.15E-10 5.15E-10 5.15E-10 5.15E-10 6 1.41E-09 2.93E-09 2.93E-09 2.93E-09 7 1.19E-10 1.19E-10 5.95E-10 1.19E-10 5.95E-10 8 1.11E-10 1.11E-10 5.56E-10 1.11E-10 5.56E-10 9 1.10E-10 1.10E-10 1.10E-10 1.10E-10 1.10E-10 10 9.70E-09 9.70E-09 9.70E-09 9.70E-09 9.70E-09 11 5.54E-10 5.54E-10 12 1.16E-10 1.16E-10 14 1.11E-09 1.11E-09 1.11E-09 1.11E-09 1.11E-09 15 9.78E-08 9.78E-08 9.78E-08 9.78E-08 9.78E-08 16 9.91E-09 9.91E-09 9.91E-09 9.91E-09 9.91E-09 17 8.02E-08 8.02E-08 8.02E-08 8.02E-08 8.02E-08 18 4.41E-10 4.41E-10 4.41E-10 4.41E-10 4.41E-10 19 5.02E-10 5.02E-10 5.02E-10 5.02E-10 5.02E-10 20 8.18E-09 8.18E-09 8.18E-09 8.18E-09 8.18E-09 24 5.31E-10 5.31E-10 25 1.41E-10 1.41E-10 1.41E-10 1.41E-10 26 5.33E-09 5.33E-09 5.33E-09 5.33E-09 27 1.11E-10 1.11E-10 1.11E-10 1.11E-10 1.11E-10 28 9.62E-09 9.62E-09 9.62E-09 9.62E-09 9.62E-09 37 1.25E-10 1.25E-10 1.25E-10 1.25E-10 38 1.21E-08 1.21E-08 1.21E-08 1.21E-08 1.21E-08 39 6.16E-10 6.16E-10 6.16E-10 6.16E-10 40 1.17E-06 1.17E-06 1.17E-06 1.17E-06 1.17E-06 41 1.23E-09 1.23E-09 1.23E-09 1.23E-09 1.23E-09 42 1.18E-08 1.18E-08 1.18E-08 1.18E-08 1.18E-08 43 1.16E-09 1.16E-09 1.16E-09 1.16E-09 1.16E-09 44 1.05E-07 1.05E-07 1.05E-07 1.05E-07 1.05E-07 45 1.13E-10 1.13E-10 47 1.15E-09 1.15E-09 1.15E-09 1.15E-09 1.15E-09 49 9.99E-10 9.99E-10 9.99E-10 9.99E-10 9.99E-10 50 1.24E-07 1.24E-07 1.24E-07 1.24E-07 1.24E-07 51 6.16E-10 1.23E-09 1.23E-09 1.23E-09 52 1.27E-09 1.27E-09 53 4.85E-09 9.71E-09 9.71E-09 9.71E-09 54 1.28E-10 1.28E-10 1.28E-10 1.28E-10 55 3.13E-09 3.13E-09 3.13E-09 6.26E-09 56 1.23E-10 1.23E-10 1.23E-10 1.23E-10 57 1.49E-10 1.49E-10 1.49E-10 1.49E-10 58 1.20E-10 1.20E-10 1.20E-10 1.20E-10 1.20E-10 59 1.13E-10 1.13E-10 1.13E-10 1.13E-10 1.13E-10 60 1.00E-08 5.00E-09 5.00E-09 5.00E-09 5.00E-09 61 1.12E-10 1.12E-10 1.12E-10 1.12E-10 1.12E-10 62 8.88E-10 8.88E-10 8.88E-10 8.88E-10 8.88E-10 63 5.06E-10 5.06E-10 5.06E-10 5.06E-10 5.06E-10 64 1.18E-10 5.92E-10 5.92E-10 5.92E-10 65 1.12E-10 1.12E-10 1.12E-10 1.12E-10 1.12E-10 66 1.16E-10 1.16E-10 1.16E-10 1.16E-10 1.16E-10 68 6.33E-10 6.33E-10 69 1.25E-10 6.23E-10 6.23E-10 6.23E-10 6.23E-10 70 1.25E-10 1.25E-10 1.25E-10 1.25E-10 1.25E-10 71 5.88E-10 5.88E-10 5.88E-10 5.88E-10 5.88E-10 79 1.07E-10 1.07E-10 80 2.96E-09 5.92E-09 5.92E-09 5.92E-09 81 5.54E-09 5.54E-09 82 9.86E-08 9.86E-08 83 8.08E-08 8.08E-08 8.08E-08 8.08E-08 8.08E-08 84 4.89E-08 4.89E-08 85 9.71E-09 9.71E-09 86 5.20E-10 5.20E-10 5.20E-10 5.20E-10 5.20E-10 88 1.22E-08 1.22E-08 1.22E-08 1.22E-08 1.22E-08 89 5.91E-07 5.91E-07 5.91E-07 5.91E-07 5.91E-07 90 1.19E-08 1.19E-08 1.19E-08 1.19E-08 1.19E-08 91 1.06E-07 1.06E-07 1.06E-07 1.06E-07 1.06E-07 94 1.52E-10 1.52E-10 1.52E-10 1.52E-10 96 1.25E-09 1.25E-09 1.25E-09 1.25E-09 98 1.29E-10 1.29E-10 104 1.17E-10 5.83E-10 5.83E-10 5.83E-10 5.83E-10 106 1.21E-09 1.21E-09 1.21E-09 1.21E-09 1.21E-09 107 1.08E-09 1.08E-09 1.08E-09 1.08E-09 1.08E-09 108 1.08E-10 1.08E-10 109 9.80E-10 9.80E-10 110 9.72E-11 9.72E-11 111 1.11E-09 1.11E-09 1.11E-09 1.11E-09 1.11E-09 112 1.03E-08 1.03E-08 113 1.04E-08 1.04E-08 1.04E-08 1.04E-08 1.04E-08 114 9.18E-09 9.18E-09 115 1.10E-10 1.10E-10 116 1.09E-10 1.09E-10 119 1.05E-08 1.05E-08 1.05E-08 1.05E-08 1.05E-08 120 4.63E-07 4.63E-07 4.63E-07 4.63E-07 4.63E-07 121 4.69E-07 4.69E-07 4.69E-07 4.69E-07 4.69E-07 122 8.30E-07 8.30E-07 8.30E-07 8.30E-07 8.30E-07 126 1.19E-10 1.19E-10 127 1.17E-10 1.17E-10 128 1.17E-09 1.17E-09 129 1.13E-08 1.13E-08 130 1.15E-09 1.15E-09 131 1.10E-07 1.10E-07 132 1.15E-09 1.15E-09 133 1.10E-07 1.10E-07 134 5.44E-10 5.44E-10 5.44E-10 5.44E-10 5.44E-10 135 4.96E-09 4.96E-09 4.96E-09 4.96E-09 4.96E-09 136 1.37E-10 1.37E-10 1.37E-10 1.37E-10 1.37E-10 137 1.17E-10 1.17E-10 1.17E-10 1.17E-10 1.17E-10 138 1.01E-09 1.01E-09 139 1.25E-09 1.25E-09 140 1.15E-09 1.15E-09 141 1.23E-10 1.23E-10 142 1.22E-09 1.22E-09 144 1.17E-09 1.17E-09 1.17E-09 1.17E-09 1.17E-09 145 1.02E-07 1.02E-07 146 1.03E-07 1.03E-07 1.03E-07 1.03E-07 1.03E-07 149 1.35E-10 1.35E-10 150 1.32E-09 1.32E-09 151 1.32E-10 1.32E-10 152 1.28E-08 1.28E-08 153 1.30E-10 1.30E-10 154 1.23E-08 1.23E-08 155 1.30E-09 1.30E-09 156 1.24E-08 1.24E-08 157 1.22E-10 1.22E-10 158 1.10E-09 1.10E-09 159 1.37E-09 1.37E-09 1.37E-09 1.37E-09 1.37E-09 160 1.09E-09 1.09E-09 161 1.18E-10 1.18E-10 1.18E-10 1.18E-10 1.18E-10 162 5.10E-09 5.10E-09 164 1.16E-08 1.16E-08 168 5.91E-10 5.91E-10 5.91E-10 5.91E-10 5.91E-10 169 1.03E-09 1.03E-09 170 5.22E-08 5.22E-08 5.22E-08 5.22E-08 5.22E-08 177 1.34E-10 1.34E-10 178 1.31E-09 1.31E-09 179 1.25E-08 1.25E-08 180 6.18E-10 6.18E-10 181 1.11E-08 1.11E-08 183 1.32E-10 1.32E-10 184 6.99E-10 6.99E-10 6.99E-10 6.99E-10 185 1.32E-08 1.32E-08 1.32E-08 1.32E-08 186 1.59E-10 1.59E-10 1.59E-10 1.59E-10 187 1.08E-09 1.08E-09 1.08E-09 1.08E-09 188 5.83E-10 5.83E-10 5.83E-10 5.83E-10 189 5.83E-10 5.83E-10 5.83E-10 5.83E-10 190 5.22E-09 5.22E-09 5.22E-09 5.22E-09 191 1.11E-09 1.11E-09 1.11E-09 1.11E-09 1.11E-09 192 5.39E-09 5.39E-09 5.39E-09 5.39E-09 5.39E-09 194 5.07E-08 5.07E-08 5.07E-08 5.07E-08 5.07E-08 195 1.02E-08 1.02E-08 1.02E-08 1.02E-08 1.02E-08 196 9.02E-06 9.02E-06 9.02E-06 9.02E-06 9.02E-06 197 9.13E-06 9.13E-06 9.13E-06 9.13E-06 9.13E-06 198 7.50E-06 7.50E-06 7.50E-06 7.50E-06 7.50E-06 201 1.26E-08 1.57E-08 1.57E-08 1.57E-08 202 1.25E-10 1.25E-10 1.25E-10 6.25E-11 6.25E-11 203 1.21E-10 1.21E-10 1.21E-10 1.21E-10 1.21E-10 204 1.13E-10 1.13E-10 1.13E-10 1.13E-10 1.13E-10 205 1.13E-10 1.13E-10 1.13E-10 1.13E-10 1.13E-10 206 4.96E-08 4.96E-08 4.96E-08 4.96E-08 4.96E-08 207 5.03E-09 5.03E-09 5.03E-09 5.03E-09 5.03E-09 208 8.11E-06 8.11E-06 8.11E-06 8.11E-06 8.11E-06 213 1.14E-10 1.14E-10 214 5.00E-09 5.00E-09 216 8.16E-08 8.16E-08 221 1.34E-09 1.34E-09

Compound 13 Compound 21 Compound 29 A-549 GI₅₀ 1.08E-09 3.34E-09 2.16E-09 TGI 3.24E-09 1.06E-08 4.32E-09 LC₅₀ 8.65E-09 1.06E-05 1.08E-08 H-T29 GI₅₀ 3.24E-10 5.31E-09 2.16E-09 TGI 3.24E-10 1.06E-07 2.16E-09 LC₅₀ 1.08E-08 1.06E-05 1.08E-06 SW-620 GI₅₀ TGI LC₅₀ MEL-28 GI₅₀ TGI LC₅₀ OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ TGI LC₅₀ DU-145 GI₅₀ TGI LC₅₀ MCF GI₅₀ TGI LC₅₀ MB-231 GI₅₀ TGI LC₅₀ HMEC-1 GI₅₀ TGI LC₅₀ LNCAP GI₅₀ TGI LC₅₀ SK-OV3 GI₅₀ TGI LC₅₀ IGROV GI₅₀ TGI LC₅₀ IGROV-ET GI₅₀ TGI LC₅₀ SK-BR3 GI₅₀ TGI LC₅₀ K-562 GI₅₀ TGI LC₅₀ PANC-1 GI₅₀ TGI LC₅₀ LOVO GI₅₀ TGI LC₅₀ LOVO-DOX GI₅₀ TGI LC₅₀ HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 30 Compound 31 Compound 32 A-549 GI₅₀ 3.29E-08 4.08E-08 2.20E-09 TGI 5.49E-08 9.17E-08 6.59E-09 LC₅₀ 3.29E-06 1.02E-06 1.10E-08 H-T29 GI₅₀ 8.78E-08 8.15E-08 1.10E-09 TGI 8.78E-08 8.15E-08 6.60E-09 LC₅₀ 1.10E-05 1.02E-05 9.88E-09 SW-620 GI₅₀ TGI LC₅₀ MEL-28 GI₅₀ TGI LC₅₀ OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ TGI LC₅₀ DU-145 GI₅₀ TGI LC₅₀ MCF GI₅₀ TGI LC₅₀ MB-231 GI₅₀ TGI LC₅₀ HMEC-1 GI₅₀ TGI LC₅₀ LNCAP GI₅₀ TGI LC₅₀ SK-OV3 GI₅₀ TGI LC₅₀ IGROV GI₅₀ TGI LC₅₀ IGROV-ET GI₅₀ TGI LC₅₀ SK-BR3 GI₅₀ TGI LC₅₀ K-562 GI₅₀ TGI LC₅₀ PANC-1 GI₅₀ TGI LC₅₀ LOVO GI₅₀ TGI LC₅₀ LOVO-DOX GI₅₀ TGI LC₅₀ HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 33 Compound 34 Compound 35 A-549 GI₅₀ 4.37E-09 7.64E-10 5.68E-09 TGI 2.50E-08 2.84E-09 7.22E-08 LC₅₀ 1.27E-05 9.06E-09 2.15E-06 H-T29 GI₅₀ 3.42E-08 8.09E-10 5.41E-09 TGI 1.25E-07 1.29E-08 1.25E-08 LC₅₀ 1.25E-05 1.27E-05 1.25E-05 SW-620 GI₅₀ TGI LC₅₀ MEL-28 GI₅₀ TGI LC₅₀ OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ TGI LC₅₀ DU-145 GI₅₀ TGI LC₅₀ MCF GI₅₀ TGI LC₅₀ MB-231 GI₅₀ TGI LC₅₀ HMEC-1 GI₅₀ TGI LC₅₀ LNCAP GI₅₀ TGI LC₅₀ SK-OV3 GI₅₀ TGI LC₅₀ IGROV GI₅₀ TGI LC₅₀ IGROV-ET GI₅₀ TGI LC₅₀ SK-BR3 GI₅₀ TGI LC₅₀ K-562 GI₅₀ TGI LC₅₀ PANC-1 GI₅₀ TGI LC₅₀ LOVO GI₅₀ TGI LC₅₀ LOVO-DOX GI₅₀ TGI LC₅₀ HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 36 Compound 46 Compound 48 A-549 GI₅₀ 6.26E-09 1.79E-07 2.72E-07 TGI 1.03E-07 4.06E-07 7.50E-07 LC₅₀ 4.14E-06 9.27E-07 3.89E-06 H-T29 GI₅₀ 5.67E-09 3.98E-07 1.97E-06 TGI 2.55E-08 1.95E-06 1.23E-05 LC₅₀ 1.27E-05 1.10E-05 1.23E-05 SW-620 GI₅₀ TGI LC₅₀ MEL-28 GI₅₀ 1.10E-06 TGI 2.87E-06 LC₅₀ 7.06E-06 OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ TGI LC₅₀ DU-145 GI₅₀ 6.14E-07 TGI 3.20E-06 LC₅₀ 1.23E-05 MCF GI₅₀ TGI LC₅₀ MB-231 GI₅₀ TGI LC₅₀ HMEC-1 GI₅₀ 1.52E-07 TGI 5.18E-07 LC₅₀ 1.10E-05 LNCAP GI₅₀ TGI LC₅₀ SK-OV3 GI₅₀ 6.14E-07 TGI 3.40E-06 LC₅₀ 1.23E-05 IGROV GI₅₀ 4.39E-07 TGI 1.78E-06 LC₅₀ 7.98E-06 IGROV-ET GI₅₀ 6.78E-07 TGI 2.93E-06 LC₅₀ 1.23E-05 SK-BR3 GI₅₀ 4.43E-07 TGI 1.54E-06 LC₅₀ 6.97E-06 K-562 GI₅₀ 2.23E-07 TGI 5.47E-07 LC₅₀ 1.23E-06 PANC-1 GI₅₀ 9.10E-07 TGI 5.10E-06 LC₅₀ 1.23E-05 LOVO GI₅₀ 7.13E-07 TGI 2.95E-06 LC₅₀ 1.23E-05 LOVO-DOX GI₅₀ 7.90E-07 TGI 4.18E-06 LC₅₀ 1.23E-05 HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 67 Compound 72 Compound 73 A-549 GI₅₀ 1.31E-09 1.12E-09 3.52E-10 TGI 3.63E-09 3.36E-09 2.35E-09 LC₅₀ 1.01E-08 7.83E-09 5.87E-09 HT-29 GI₅₀ 7.41E-10 2.24E-09 9.39E-10 TGI 5.59E-09 7.83E-09 7.04E-09 LC₅₀ 1.29E-05 1.12E-08 1.06E-08 SW-620 GI₅₀ 2.24E-09 3.52E-10 TGI 3.36E-09 1.17E-09 LC₅₀ 1.12E-08 9.39E-09 MEL-28 GI₅₀ 4.11E-10 2.24E-09 8.22E-10 TGI 9.90E-10 3.36E-09 9.39E-10 LC₅₀ 6.24E-09 7.83E-09 3.52E-09 OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ 2.24E-09 3.52E-10 TGI 4.47E-09 7.04E-10 LC₅₀ 1.12E-08 3.52E-09 DU-145 GI₅₀ 4.33E-10 2.24E-09 2.35E-10 TGI 8.61E-10 3.36E-09 3.52E-10 LC₅₀ 4.47E-06 8.95E-09 9.39E-10 MCF GI₅₀ 2.24E-09 7.04E-10 TGI 4.47E-09 3.52E-09 LC₅₀ 1.12E-08 1.17E-08 MB-231 GI₅₀ 2.24E-09 2.35E-10 TGI 3.36E-09 4.69E-11 LC₅₀ 1.12E-08 1.17E-09 HMEC-1 GI₅₀ 1.02E-09 TGI 8.49E-09 LC₅₀ 5.05E-06 LNCAP GI₅₀ 3.07E-10 TGI 5.09E-10 LC₅₀ 8.44E-10 SK-OV3 GI₅₀ 3.85E-10 TGI 8.52E-10 LC₅₀ 7.94E-06 IGROV GI₅₀ 2.66E-10 TGI 5.67E-10 LC₅₀ 1.21E-09 IGROV-ET GI₅₀ 1.88E-09 TGI 7.02E-09 LC₅₀ 4.96E-06 SK-BR3 GI₅₀ 3.94E-10 TGI 1.11E-09 LC₅₀ 7.48E-09 K-562 GI₅₀ 1.18E-10 TGI 2.85E-10 LC₅₀ 8.00E-10 PANC-1 GI₅₀ 4.43E-10 TGI 1.09E-09 LC₅₀ 2.67E-06 LOVO GI₅₀ 6.02E-10 TGI 3.34E-09 LC₅₀ 1.77E-08 LOVO-DOX GI₅₀ 4.21E-09 TGI 3.65E-08 LC₅₀ 1.28E-05 HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 74 Compound 75 Compound 76 A-549 GI₅₀ 3.99E-10 4.26E-09 2.06E-09 TGI 9.04E-10 8.23E-09 4.31E-09 LC₅₀ 6.38E-09 4.90E-08 9.07E-09 HT-29 GI₅₀ 3.54E-10 3.89E-09 1.28E-09 TGI 8.35E-10 1.18E-08 6.18E-09 LC₅₀ 1.04E-05 1.20E-07 4.52E-06 SW-620 GI₅₀ TGI LC₅₀ MEL-28 GI₅₀ 2.75E-10 2.00E-09 6.22E-10 TGI 5.22E-10 4.82E-09 2.51E-09 LC₅₀ 9.94E-10 1.17E-08 8.28E-09 OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ TGI LC₅₀ DU-145 GI₅₀ 3.66E-10 5.63E-10 2.49E-10 TGI 7.61E-10 9.47E-10 6.16E-10 LC₅₀ 2.79E-06 8.33E-06 2.14E-06 MCF GI₅₀ TGI LC₅₀ MB-231 GI₅₀ TGI LC₅₀ HMEC-1 GI₅₀ 5.98E-10 6.97E-09 1.83E-09 TGI 1.45E-08 5.77E-08 6.55E-09 LC₅₀ 4.70E-06 1.20E-05 1.86E-07 LNCAP GI₅₀ 1.29E-10 5.79E-10 2.17E-10 TGI 2.69E-10 8.31E-10 4.40E-10 LC₅₀ 5.64E-10 1.19E-09 8.91E-10 SK-OV3 GI₅₀ 2.48E-10 2.19E-09 2.93E-10 TGI 4.76E-10 1.04E-08 8.93E-10 LC₅₀ 1.11E-09 1.20E-05 4.81E-06 IGROV GI₅₀ 2.37E-10 5.20E-10 1.92E-10 TGI 4.65E-10 1.63E-09 4.56E-10 LC₅₀ 9.11E-10 1.00E-08 1.66E-09 IGROV-ET GI₅₀ 1.76E-09 3.38E-09 1.52E-09 TGI 4.69E-09 6.58E-09 3.92E-09 LC₅₀ 1.97E-08 1.20E-08 2.10E-08 SK-BR3 GI₅₀ 2.75E-10 1.20E-09 3.37E-10 TGI 7.64E-10 3.21E-09 1.24E-09 LC₅₀ 4.18E-09 8.58E-09 6.17E-09 K-562 GI₅₀ 5.26E-11 3.64E-10 2.78E-12 TGI 2.10E-10 7.42E-10 3.78E-11 LC₅₀ 6.61E-10 4.16E-09 3.51E-10 PANC-1 GI₅₀ 3.13E-10 3.04E-09 1.22E-09 TGI 6.77E-10 8.45E-09 4.68E-09 LC₅₀ 2.55E-09 3.59E-08 4.41E-08 LOVO GI₅₀ 3.69E-10 2.25E-09 1.03E-09 TGI 1.16E-09 4.82E-09 3.30E-09 LC₅₀ 1.10E-08 1.20E-08 1.08E-08 LOVO-DOX GI₅₀ 6.31E-09 4.26E-08 1.39E-08 TGI 6.33E-08 1.23E-07 4.70E-08 LC₅₀ 3.59E-07 1.20E-05 1.07E-07 HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 77 Compound 78 Compound 87 A-549 GI₅₀ 2.11E-09 9.59E-09 2.38E-08 TGI 3.64E-09 1.99E-08 4.77E-08 LC₅₀ 6.29E-09 4.11E-08 9.58E-08 HT-29 GI₅₀ 2.96E-09 1.71E-08 2.44E-08 TGI 9.52E-09 1.10E-07 1.12E-07 LC₅₀ 1.01E-05 8.19E-06 3.80E-07 SW-620 GI₅₀ TGI LC₅₀ MEL-28 GI₅₀ 2.66E-10 2.15E-09 1.92E-08 TGI 5.06E-10 4.48E-09 4.57E-08 LC₅₀ 9.62E-10 1.69E-08 1.09E-07 OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ TGI LC₅₀ DU-145 GI₅₀ 4.88E-10 3.21E-09 1.35E-08 TGI 1.45E-09 8.52E-09 5.22E-08 LC₅₀ 1.01E-05 8.19E-06 1.80E-07 MCF GI₅₀ TGI LC₅₀ MB-231 GI₅₀ TGI LC₅₀ HMEC-1 GI₅₀ 5.28E-09 2.83E-08 1.67E-08 TGI 5.28E-08 2.35E-07 9.65E-08 LC₅₀ 1.01E-05 8.19E-06 1.27E-05 LNCAP GI₅₀ 3.28E-10 2.74E-09 4.73E-09 TGI 6.12E-10 4.05E-09 1.12E-08 LC₅₀ 1.58E-09 5.99E-09 4.05E-08 SK-OV3 GI₅₀ 2.55E-09 3.79E-09 2.16E-08 TGI 7.76E-09 6.27E-08 6.56E-08 LC₅₀ 1.01E-05 8.19E-06 8.99E-06 IGROV GI₅₀ 4.54E-10 2.38E-09 4.80E-09 TGI 1.53E-09 6.27E-09 1.63E-08 LC₅₀ 8.82E-09 5.39E-08 8.04E-08 IGROV-ET GI₅₀ 4.22E-09 1.14E-07 2.84E-08 TGI 9.57E-08 7.42E-07 7.77E-08 LC₅₀ 3.03E-07 8.19E-06 5.84E-06 SK-BR3 GI₅₀ 4.75E-10 4.31E-09 1.65E-08 TGI 2.04E-09 1.70E-08 4.08E-08 LC₅₀ 8.12E-09 6.33E-08 1.01E-07 K-562 GI₅₀ 2.77E-10 1.24E-09 8.71E-10 TGI 7.77E-10 2.56E-09 2.96E-09 LC₅₀ 3.79E-08 7.50E-09 7.15E-09 PANC-1 GI₅₀ 3.27E-09 5.42E-09 2.53E-08 TGI 9.14E-09 3.24E-08 7.39E-08 LC₅₀ 6.30E-06 4.90E-06 8.76E-07 LOVO GI₅₀ 1.91E-09 1.07E-08 2.27E-08 TGI 3.96E-09 2.83E-08 5.27E-08 LC₅₀ 8.21E-09 7.43E-08 1.23E-07 LOVO-DOX GI₅₀ 3.13E-08 8.85E-08 3.87E-08 TGI 9.39E-08 8.77E-07 1.42E-07 LC₅₀ 1.01E-05 8.19E-06 1.27E-05 HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 92 Compound 93 Compound 95 A-549 GI₅₀ 3.33E-09 4.63E-10 2.68E-08 TGI 7.77E-09 2.90E-09 5.55E-08 LC₅₀ 3.33E-08 1.29E-08 1.47E-07 HT-29 GI₅₀ 1.11E-09 6.35E-10 4.04E-08 TGI 1.11E-09 1.29E-08 1.27E-07 LC₅₀ 5.55E-08 1.29E-05 1.20E-05 SW-620 GI₅₀ TGI LC₅₀ MEL-28 GI₅₀ 2.81E-10 2.52E-08 TGI 6.24E-10 4.58E-08 LC₅₀ 3.58E-09 8.32E-08 OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ TGI LC₅₀ DU-145 GI₅₀ 3.31E-10 3.76E-08 TGI 6.30E-10 8.92E-08 LC₅₀ 1.29E-09 1.01E-06 MCF GI₅₀ TGI LC₅₀ MB-231 GI₅₀ TGI LC₅₀ HMEC-1 GI₅₀ 3.70E-11 9.36E-09 TGI 1.55E-10 2.80E-08 LC₅₀ 4.87E-10 7.56E-08 LNCAP GI₅₀ 2.85E-09 1.77E-08 TGI 6.77E-09 3.41E-08 LC₅₀ 1.29E-07 6.60E-08 SK-OV3 GI₅₀ 4.09E-10 2.81E-08 TGI 1.29E-09 6.59E-08 LC₅₀ 1.29E-05 3.68E-07 IGROV GI₅₀ 2.14E-10 2.80E-08 TGI 6.46E-10 6.67E-08 LC₅₀ 1.29E-07 1.09E-06 IGROV-ET GI₅₀ 2.15E-08 5.05E-08 TGI 1.31E-07 1.16E-07 LC₅₀ 1.29E-05 1.20E-05 SK-BR3 GI₅₀ 4.45E-10 2.98E-08 TGI 1.96E-09 7.62E-08 LC₅₀ 9.50E-09 5.22E-07 K-562 GI₅₀ 6.11E-10 1.53E-08 TGI 1.29E-08 5.30E-08 LC₅₀ 9.54E-06 2.22E-06 PANC-1 GI₅₀ 3.14E-10 3.88E-08 TGI 1.29E-09 1.08E-07 LC₅₀ 1.29E-05 1.09E-06 LOVO GI₅₀ 7.68E-10 2.62E-08 TGI 4.58E-09 5.40E-08 LC₅₀ 1.29E-05 1.11E-07 LOVO-DOX GI₅₀ 7.71E-09 2.40E-07 TGI 9.87E-08 8.68E-07 LC₅₀ 1.29E-05 1.20E-05 HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 97 Compound 99 Compound 100 A5-49 GI₅₀ 3.48E-10 4.35E-08 2.98E-08 TGI 9.28E-10 9.96E-08 6.20E-08 LC₅₀ 3.48E-09 1.03E-05 1.12E-07 HT-29 GI₅₀ 9.28E-10 3.43E-08 3.50E-08 TGI 2.32E-09 1.03E-07 8.07E-08 LC₅₀ 9.28E-09 1.03E-05 1.11E-05 SW-620 GI₅₀ 5.80E-10 TGI 2.32E-09 LC₅₀ 9.28E-09 MEL-28 GI₅₀ 3.48E-10 2.65E-08 TGI 9.28E-10 5.04E-08 LC₅₀ 3.48E-09 9.59E-08 OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ 5.80E-10 TGI 2.32E-09 LC₅₀ 9.28E-09 DU-145 GI₅₀ 2.32E-10 4.31E-08 TGI 3.48E-10 1.03E-07 LC₅₀ 9.28E-10 8.32E-06 MCF GI₅₀ 1.16E-09 TGI 3.48E-09 LC₅₀ 1.16E-08 MB-231 GI₅₀ 3.48E-10 TGI 6.96E-10 LC₅₀ 3.48E-08 HMEC-1 GI₅₀ 2.75E-08 TGI 5.14E-08 LC₅₀ 9.61E-08 LNCAP GI₅₀ 2.15E-08 TGI 3.79E-08 LC₅₀ 6.65E-08 SK-OV3 GI₅₀ 2.82E-08 TGI 5.74E-08 LC₅₀ 1.11E-07 IGROV GI₅₀ 3.51E-08 TGI 6.54E-08 LC₅₀ 9.15E-07 IGROV-ET GI₅₀ 6.32E-08 TGI 7.41E-07 LC₅₀ 1.11E-05 SK-BR3 GI₅₀ 4.05E-08 TGI 9.87E-08 LC₅₀ 1.72E-06 K-562 GI₅₀ 3.64E-08 TGI 6.20E-08 LC₅₀ 1.06E-07 PANC-1 GI₅₀ 4.14E-08 TGI 1.14E-08 LC₅₀ 8.32E-06 LOVO GI₅₀ 2.44E-08 TGI 4.48E-08 LC₅₀ 8.23E-08 LOVO-DOX GI₅₀ 3.92E-07 TGI 2.73E-06 LC₅₀ 1.11E-05 HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 101 Compound 102 Compound 118 A5-49 GI₅₀ 3.69E-09 1.52E-07 3.34E-09 TGI 6.52E-09 4.24E-07 8.90E-08 LC₅₀ 1.15E-08 1.19E-06 2.22E-06 HT-29 GI₅₀ 3.57E-09 8.70E-08 7.79E-09 TGI 1.03E-08 2.19E-06 7.79E-09 LC₅₀ 1.29E-05 1.24E-05 1.11E-05 SW-620 GI₅₀ TGI LC₅₀ MEL-28 GI₅₀ 3.35E-09 3.79E-08 TGI 7.02E-09 6.89E-08 LC₅₀ 2.60E-08 1.28E-07 OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ TGI LC₅₀ DU-145 GI₅₀ 3.74E-09 3.98E-08 TGI 7.46E-09 7.84E-08 LC₅₀ 1.79E-08 1.24E-07 MCF GI₅₀ TGI LC₅₀ MB-231 GI₅₀ TGI LC₅₀ HMEC-1 GI₅₀ 3.05E-09 TGI 1.17E-08 LC₅₀ 1.29E-05 LNCAP GI₅₀ 2.50E-09 1.75E-08 TGI 4.40E-09 4.09E-08 LC₅₀ 7.71E-09 9.54E-08 SK-OV3 GI₅₀ 4.49E-09 4.13E-08 TGI 9.77E-09 1.10E-07 LC₅₀ 1.29E-05 1.24E-07 IGROV GI₅₀ 2.50E-09 3.53E-08 TGI 5.17E-09 7.63E-08 LC₅₀ 1.07E-08 1.34E-07 IGROV-ET GI₅₀ 3.05E-08 1.01E-07 TGI 6.88E-08 1.53E-06 LC₅₀ 2.46E-07 7.81E-06 SK-BR3 GI₅₀ 2.63E-09 TGI 6.44E-09 LC₅₀ 4.68E-08 K-562 GI₅₀ 2.50E-10 1.02E-08 TGI 6.20E-10 4.35E-08 LC₅₀ 1.92E-08 1.26E-07 PANC-1 GI₅₀ 5.66E-09 5.54E-08 TGI 2.27E-08 1.39E-07 LC₅₀ 1.34E-06 1.24E-05 LOVO GI₅₀ 1.34E-08 6.98E-08 TGI 4.68E-08 4.58E-07 LC₅₀ 2.19E-07 1.24E-05 LOVO-DOX GI₅₀ 2.51E-07 4.17E-07 TGI 9.29E-07 1.02E-06 LC₅₀ 1.29E-05 1.24E-05 HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 123 Compound 124 Compound 125 A-549 GI₅₀ 7.33E-09 6.87E-09 1.00E-09 TGI 2.09E-08 7.33E-07 3.00E-09 LC₅₀ 7.33E-08 7.80E-06 8.00E-09 HT-29 GI₅₀ 3.14E-09 3.56E-09 2.00E-10 TGI 3.14E-09 7.80E-08 2.00E-10 LC₅₀ 3.14E-08 7.80E-06 3.00E-09 SW-620 GI₅₀ TGI LC₅₀ MEL-28 GI₅₀ TGI LC₅₀ OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ TGI LC₅₀ DU-145 GI₅₀ TGI LC₅₀ MCF GI₅₀ TGI LC₅₀ MB-231 GI₅₀ TGI LC₅₀ HMEC-1 GI₅₀ TGI LC₅₀ LNCAP GI₅₀ TGI LC₅₀ SK-OV3 GI₅₀ TGI LC₅₀ IGROV GI₅₀ TGI LC₅₀ IGROV-ET GI₅₀ TGI LC₅₀ SK-BR3 GI₅₀ TGI LC₅₀ K-562 GI₅₀ TGI LC₅₀ PANC-1 GI₅₀ TGI LC₅₀ LOVO GI₅₀ TGI LC₅₀ LOVO-DOX GI₅₀ TGI LC₅₀ HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 143 Compound 147 Compound 148 A-549 GI₅₀ 2.16E-08 3.26E-08 2.55E-07 TGI 4.32E-08 6.84E-08 5.19E-07 LC₅₀ 1.08E-07 1.05E-06 2.88E-06 HT-29 GI₅₀ 1.08E-08 1.97E-08 1.40E-07 TGI 1.08E-08 1.05E-07 3.32E-07 LC₅₀ 1.08E-05 1.05E-05 7.86E-07 SW-620 GI₅₀ TGI LC₅₀ MEL-28 GI₅₀ TGI LC₅₀ OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ TGI LC₅₀ DU-145 GI₅₀ TGI LC₅₀ MCF GI₅₀ TGI LC₅₀ MB-231 GI₅₀ TGI LC₅₀ HMEC-1 GI₅₀ TGI LC₅₀ LNCAP GI₅₀ TGI LC₅₀ SK-OV3 GI₅₀ TGI LC₅₀ IGROV GI₅₀ TGI LC₅₀ IGROV-ET GI₅₀ TGI LC₅₀ SK-BR3 GI₅₀ TGI LC₅₀ K-562 GI₅₀ TGI LC₅₀ PANC-1 GI₅₀ TGI LC₅₀ LOVO GI₅₀ TGI LC₅₀ LOVO-DOX GI₅₀ TGI LC₅₀ HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 163 Compound 165 Compound 166 A-549 GI₅₀ 3.80E-10 1.24E-10 9.88E-10 TGI 2.53E-09 3.73E-10 3.70E-09 LC₅₀ 8.86E-09 1.24E-09 9.88E-09 HT-29 GI₅₀ 3.80E-10 2.49E-10 1.23E-09 TGI 1.14E-09 3.73E-10 3.70E-09 LC₅₀ 3.80E-09 9.95E-10 9.88E-09 SW-620 GI₅₀ 3.80E-10 1.24E-10 3.70E-10 TGI 2.53E-09 4.98E-10 3.70E-09 LC₅₀ 1.01E-08 6.22E-09 1.11E-08 MEL-28 GI₅₀ 2.53E-10 1.24E-10 4.94E-10 TGI 1.01E-09 3.73E-10 1.23E-09 LC₅₀ 3.80E-09 9.95E-10 4.94E-09 OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ 3.80E-10 2.49E-10 1.23E-09 TGI 1.27E-09 6.22E-10 4.94E-09 LC₅₀ 1.27E-08 2.49E-09 1.11E-08 DU-145 GI₅₀ 2.53E-10 2.49E-11 3.70E-10 TGI 3.80E-10 6.22E-11 4.94E-10 LC₅₀ 1.01E-09 2.49E-10 1.23E-09 MCF GI₅₀ 2.53E-09 9.95E-10 2.47E-09 TGI 5.06E-09 4.98E-09 8.64E-09 LC₅₀ 1.27E-08 1.12E-08 1.11E-08 MB-231 GI₅₀ 2.53E-10 2.49E-10 4.94E-10 TGI 6.33E-10 1.24E-09 2.47E-09 LC₅₀ 1.27E-08 1.12E-08 1.23E-08 HMEC-1 GI₅₀ TGI LC₅₀ LNCAP GI₅₀ TGI LC₅₀ SK-OV3 GI₅₀ TGI LC₅₀ IGROV GI₅₀ TGI LC₅₀ IGROV-ET GI₅₀ TGI LC₅₀ SK-BR3 GI₅₀ TGI LC₅₀ K-562 GI₅₀ TGI LC₅₀ PANC-1 GI₅₀ TGI LC₅₀ LOVO GI₅₀ TGI LC₅₀ LOVO-DOX GI₅₀ TGI LC₅₀ HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 167 Compound 171 Compound 172 A-549 GI₅₀ 2.83E-08 2.28E-08 2.41E-07 TGI 6.54E-08 4.68E-08 4.59E-07 LC₅₀ 4.82E-07 9.60E-08 8.53E-07 HT-29 GI₅₀ 2.89E-08 3.91E-09 3.88E-08 TGI 1.51E-07 3.24E-08 1.43E-07 LC₅₀ 1.09E-05 1.06E-05 8.53E-06 SW-620 GI₅₀ TGI LC₅₀ MEL-28 GI₅₀ 2.38E-08 5.65E-09 1.31E-09 TGI 5.06E-08 2.33E-08 3.22E-09 LC₅₀ 1.07E-07 1.02E-07 7.97E-09 OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ TGI LC₅₀ DU-145 GI₅₀ 4.88E-08 5.05E-09 3.79E-08 TGI 1.01E-07 2.96E-08 8.31E-08 LC₅₀ 1.09E-05 1.06E-05 8.53E-06 MCF GI₅₀ TGI LC₅₀ MB-231 GI₅₀ TGI LC₅₀ HMEC-1 GI₅₀ 5.15E-08 2.94E-09 4.32E-07 TGI 3.49E-07 6.90E-09 8.53E-06 LC₅₀ 1.09E-05 1.06E-05 8.53E-06 LNCAP GI₅₀ 1.97E-08 1.66E-09 2.77E-08 TGI 3.80E-08 3.14E-09 4.31E-08 LC₅₀ 7.36E-08 5.94E-09 6.68E-08 SE-OV3 GI₅₀ 4.02E-08 6.89E-09 2.19E-07 TGI 1.48E-07 9.73E-08 5.09E-07 LC₅₀ 1.09E-05 1.06E-05 8.53E-07 IGROV GI₅₀ 6.46E-09 1.93E-09 1.42E-08 TGI 2.49E-08 4.12E-09 3.01E-08 LC₅₀ 8.92E-08 8.80E-09 6.36E-08 IGROV-ET GI₅₀ 7.76E-08 2.25E-07 1.65E-07 TGI 9.05E-07 7.08E-07 4.18E-07 LC₅₀ 5.24E-06 1.06E-05 8.53E-07 SE-BR3 GI₅₀ 1.76E-08 2.47E-09 5.02E-08 TGI 5.19E-08 6.54E-09 2.00E-07 LC₅₀ 2.38E-07 3.75E-08 7.85E-07 E-562 GI₅₀ 7.00E-09 2.43E-10 6.03E-09 TGI 9.64E-09 4.88E-10 9.98E-09 LC₅₀ 7.17E-08 9.82E-10 3.53E-08 PANC-1 GI₅₀ 4.65E-08 7.30E-09 3.26E-07 TGI 1.09E-07 4.63E-08 8.34E-07 LC₅₀ 1.09E-05 1.06E-06 8.53E-06 LOVO GI₅₀ 3.36E-08 2.37E-08 2.26E-07 TGI 6.74E-08 7.66E-08 4.61E-07 LC₅₀ 1.90E-07 1.06E-05 8.53E-07 LOVO-DOX GI₅₀ 4.16E-07 9.38E-07 2.88E-06 TGI 1.58E-06 1.23E-06 7.23E-06 LC₅₀ 1.09E-05 1.06E-05 8.53E-06 HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 173 Compound 174 Compound 175 A-549 GI₅₀ 3.26E-09 9.80E-10 2.25E-09 TGI 4.35E-09 2.94E-09 4.24E-09 LC₅₀ 1.09E-08 9.80E-09 7.97E-09 HT-29 GI₅₀ 2.17E-09 1.96E-09 4.15E-09 TGI 6.52E-09 6.86E-09 1.54E-08 LC₅₀ 9.78E-09 9.80E-09 1.01E-05 SW-620 GI₅₀ 3.26E-09 9.80E-10 TGI 6.52E-09 6.86E-09 LC₅₀ 2.17E-08 6.86E-07 MEL-28 GI₅₀ 2.17E-09 1.96E-09 3.28E-09 TGI 5.43E-09 4.90E-09 6.63E-09 LC₅₀ 1.09E-08 9.80E-09 2.52E-08 OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ 2.17E-09 1.96E-09 TGI 4.35E-09 3.92E-09 LC₅₀ 2.17E-08 9.80E-09 DU-145 GI₅₀ 1.09E-09 2.94E-10 3.67E-09 TGI 2.17E-09 9.80E-10 9.20E-09 LC₅₀ 3.26E-09 3.92E-09 1.01E-05 MCF GI₅₀ 3.26E-09 3.92E-09 TGI 9.78E-09 1.96E-08 LC₅₀ 1.09E-07 8.82E-08 MB-231 GI₅₀ 2.17E-09 9.80E-10 TGI 7.61E-09 5.88E-09 LC₅₀ 2.17E-08 9.80E-08 HMEC-1 GI₅₀ 3.54E-09 TGI 1.29E-08 LC₅₀ 1.01E-05 LNCAP GI₅₀ 3.82E-10 TGI 1.12E-09 LC₅₀ 3.64E-09 SK-OV3 GI₅₀ 3.56E-09 TGI 8.77E-09 LC₅₀ 1.01E-05 IGROV GI₅₀ 6.41E-10 TGI 2.37E-09 LC₅₀ 8.13E-09 IGROV-ET GI₅₀ 3.97E-09 TGI 9.56E-09 LC₅₀ 1.72E-06 SK-BR3 GI₅₀ 1.31E-09 TGI 3.78E-09 LC₅₀ 1.32E-08 K-562 GI₅₀ 2.93E-10 TGI 4.76E-10 LC₅₀ 7.75E-10 PANC-1 GI₅₀ 4.38E-09 TGI 1.33E-08 LC₅₀ 1.01E-05 LOVO GI₅₀ 2.30E-09 TGI 4.38E-09 LC₅₀ 8.33E-09 LOVO-DOX GI₅₀ 4.33E-08 TGI 1.55E-07 LC₅₀ 1.01E-05 HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 176 Compound 182 Et-701 A-549 GI₅₀ 2.75E-09 4.09E-10 2.99E-09 TGI 6.01E-09 1.36E-09 7.06E-09 LC₅₀ 1.12E-08 6.81E-08 1.39E-08 HT-29 GI₅₀ 3.83E-09 2.72E-10 4.24E-09 TGI 7.96E-09 1.09E-09 3.72E-08 LC₅₀ 1.12E-05 1.36E-09 9.56E-06 SW-620 GI₅₀ 1.09E-09 TGI 4.09E-09 LC₅₀ 1.36E-08 MEL-28 GI₅₀ 2.58E-08 4.09E-10 9.74E-09 TGI 4.97E-08 1.36E-09 3.50E-08 LC₅₀ 9.56E-08 5.45E-09 1.22E-07 OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ 4.09E-10 TGI 1.36E-09 LC₅₀ 5.45E-09 DU-145 GI₅₀ 5.24E-09 2.72E-10 4.04E-09 TGI 1.10E-08 4.09E-10 9.70E-09 LC₅₀ 8.36E-06 1.09E-09 2.97E-06 MCF GI₅₀ 2.72E-09 TGI 5.45E-09 LC₅₀ 1.36E-08 MB-231 GI₅₀ 2.72E-10 TGI 6.81E-10 LC₅₀ 8.17E-09 HMEC-1 GI₅₀ 3.46E-09 3.99E-09 TGI 1.48E-07 1.35E-08 LC₅₀ 1.12E-05 4.57E-06 LNCAP GI₅₀ 1.62E-09 3.24E-10 TGI 3.25E-09 1.56E-09 LC₅₀ 6.49E-09 5.28E-09 SK-OV3 GI₅₀ 3.26E-09 2.10E-09 TGI 8.07E-09 1.08E-08 LC₅₀ 1.10E-08 9.85E-06 IGROV GI₅₀ 1.74E-09 2.33E-09 TGI 4.30E-09 5.08E-09 LC₅₀ 1.07E-08 1.11E-08 IGROV-ET GI₅₀ 4.88E-09 1.64E-08 TGI 3.38E-08 7.78E-08 LC₅₀ 3.45E-06 3.75E-06 SK-BR3 GI₅₀ 2.70E-09 2.21E-09 TGI 7.73E-09 6.25E-09 LC₅₀ 4.06E-08 2.75E-08 K-562 GI₅₀ 7.37E-10 1.33E-09 TGI 1.52E-09 3.50E-09 LC₅₀ 6.89E-09 1.13E-08 PANC-1 GI₅₀ 5.31E-09 4.61E-09 TGI 1.97E-08 1.19E-08 LC₅₀ 3.20E-06 2.06E-07 LOVO GI₅₀ 1.11E-08 4.56E-09 TGI 5.12E-08 1.18E-08 LC₅₀ 1.12E-07 3.75E-06 LOVO-DOX GI₅₀ 4.73E-08 5.06E-08 TGI 1.15E-06 5.46E-07 LC₅₀ 1.12E-05 1.39E-05 HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 193 Compound 200 Compound 209 A-549 GI₅₀ 4.01E-10 2.30E-08 9.09E-11 TGI 4.01E-09 3.45E-08 3.90E-10 LC₅₀ 1.00E-07 1.15E-07 1.17E-09 HT-29 GI₅₀ 1.00E-10 2.30E-08 7.79E-11 TGI 2.01E-08 8.05E-09 3.90E-10 LC₅₀ 2.01E-05 1.15E-06 1.17E-09 SW-620 GI₅₀ 7.79E-11 TGI 3.90E-10 LC₅₀ 1.30E-09 MEL-28 GI₅₀ 6.49E-11 TGI 2.60E-10 LC₅₀ 1.30E-09 OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ 1.30E-10 TGI 3.90E-10 LC₅₀ 1.30E-09 DU-145 GI₅₀ 1.30E-11 TGI 3.90E-11 LC₅₀ 1.30E-10 MCF GI₅₀ 2.60E-10 TGI 7.79E-10 LC₅₀ 5.19E-09 MB-231 GI₅₀ 1.30E-11 TGI 2.60E-10 LC₅₀ 1.30E-09 HMEC-1 GI₅₀ TGI LC₅₀ LNCAP GI₅₀ TGI LC₅₀ SK-OV3 GI₅₀ TGI LC₅₀ IGROV GI₅₀ TGI LC₅₀ IGROV-ET GI₅₀ TGI LC₅₀ SK-BR3 GI₅₀ TGI LC₅₀ K-562 GI₅₀ TGI LC₅₀ PANC-1 GI₅₀ TGI LC₅₀ LOVO GI₅₀ TGI LC₅₀ LOVO-DOX GI₅₀ TGI LC₅₀ HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 210 Compound 211 Compound 212 A-549 GI₅₀ 6.33E-14 3.67E-12 9.11E-09 TGI 5.06E-13 6.11E-09 2.28E-08 LC₅₀ 3.80E-05 6.11E-05 1.14E-07 HT-29 GI₅₀ 6.33E-14 1.22E-12 2.28E-09 TGI 6.33E-08 1.22E-12 4.56E-09 LC₅₀ 6.33E-05 6.11E-05 1.14E-08 SW-620 GI₅₀ 2.28E-11 TGI 1.14E-08 LC₅₀ 2.28E-06 MEL-28 GI₅₀ 1.14E-09 TGI 3.42E-09 LC₅₀ 9.11E-09 OVCAR GI₅₀ 3.42E-10 TGI 3.42E-09 LC₅₀ 2.28E-06 A-498 GI₅₀ 2.28E-09 TGI 1.14E-08 LC₅₀ 1.14E-06 DU-145 GI₅₀ 1.14E-10 TGI 6.83E-10 LC₅₀ 1.14E-08 MCF GI₅₀ 3.42E-10 TGI 1.14E-08 LC₅₀ 3.42E-07 MB-231 GI₅₀ 2.28E-10 TGI 5.69E-09 LC₅₀ 1.14E-07 HMEC-1 GI₅₀ TGI LC₅₀ LNCAP GI₅₀ TGI LC₅₀ SK-OV3 GI₅₀ TGI LC₅₀ IGROV GI₅₀ TGI LC₅₀ IGROV-ET GI₅₀ TGI LC₅₀ SK-BR3 GI₅₀ TGI LC₅₀ K-562 GI₅₀ TGI LC₅₀ PANC-1 GI₅₀ TGI LC₅₀ LOVO GI₅₀ TGI LC₅₀ LOVO-DOX GI₅₀ TGI LC₅₀ HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 215 Compound 217 Compound 219 A-549 GI₅₀ 9.24E-08 2.10E-09 8.24E-09 TGI 1.01E-05 6.16E-09 1.65E-06 LC₅₀ 1.01E-05 4.57E-08 1.65E-05 H-T29 GI₅₀ 8.68E-08 1.31E-08 8.24E-08 TGI 1.01E-05 1.31E-05 1.65E-06 LC₅₀ 1.01E-05 1.31E-05 1.65E-05 SW-620 GI₅₀ TGI LC₅₀ MEL-28 GI₅₀ 1.97E-08 5.37E-10 TGI 4.54E-08 1.48E-09 LC₅₀ 1.19E-07 9.39E-09 OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ TGI LC₅₀ DU-145 GI₅₀ 4.22E-08 5.03E-10 TGI 8.06E-08 8.77E-10 LC₅₀ 1.01E-05 1.31E-09 MCF GI₅₀ TGI LC₅₀ MB-231 GI₅₀ TGI LC₅₀ HMEC-1 GI₅₀ 6.76E-10 1.82E-10 TGI 7.95E-10 4.08E-10 LC₅₀ 1.01E-09 9.19E-10 LNCAP GI₅₀ 3.65E-08 3.44E-09 TGI 5.50E-08 9.78E-09 LC₅₀ 1.01E-07 6.60E-06 SK-OV3 GI₅₀ 3.45E-08 4.76E-10 TGI 1.29E-07 1.31E-09 LC₅₀ 1.01E-05 1.31E-05 IGROV GI₅₀ 2.68E-08 2.63E-08 TGI 5.82E-08 6.35E-08 LC₅₀ 1.01E-07 1.31E-07 IGROV-ET GI₅₀ 2.87E-07 2.44E-08 TGI 7.32E-07 1.31E-07 LC₅₀ 1.01E-05 1.31E-05 SK-BR3 GI₅₀ 1.62E-08 4.94E-10 TGI 4.85E-08 2.14E-09 LC₅₀ 3.88E-07 8.34E-09 K-562 GI₅₀ 3.39E-07 3.68E-10 TGI 2.79E-06 1.42E-09 LC₅₀ 1.01E-05 4.27E-06 PANC-1 GI₅₀ 2.92E-08 6.05E-10 TGI 1.74E-07 9.32E-09 LC₅₀ 1.01E-05 1.31E-05 LOVO GI₅₀ 2.35E-08 1.38E-09 TGI 5.19E-08 5.47E-09 LC₅₀ 1.01E-07 1.31E-08 LOVO-DOX GI₅₀ 6.07E-07 3.85E-08 TGI 1.01E-05 1.31E-07 LC₅₀ 1.01E-05 1.31E-05 HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Compound 220 Compound 223 Compound 224 A-549 GI₅₀ 1.32E-07 3.87E-09 5.32E-09 TGI 3.96E-07 1.01E-08 1.10E-08 LC₅₀ 6.61E-06 1.28E-05 1.29E-05 H-T29 GI₅₀ 1.32E-07 6.54E-09 5.19E-09 TGI 5.28E-07 1.28E-07 1.36E-08 LC₅₀ 1.32E-06 1.28E-05 1.26E-05 SW-620 GI₅₀ TGI LC₅₀ MEL-28 GI₅₀ 2.79E-09 TGI 5.35E-09 LC₅₀ 1.02E-08 OVCAR GI₅₀ TGI LC₅₀ A-498 GI₅₀ TGI LC₅₀ DU-145 GI₅₀ 5.07E-09 TGI 1.08E-08 LC₅₀ 3.32E-08 MCF GI₅₀ TGI LC₅₀ MB-231 GI₅₀ TGI LC₅₀ HMEC-1 GI₅₀ 1.01E-09 TGI 2.58E-09 LC₅₀ 6.91E-09 LNCAP GI₅₀ 1.83E-09 TGI 3.62E-09 LC₅₀ 7.16E-09 SK-OV3 GI₅₀ 4.47E-09 TGI 8.33E-09 LC₅₀ 6.60E-06 IGROV GI₅₀ 3.55E-09 TGI 8.61E-09 LC₅₀ 4.35E-06 IGROV-ET GI₅₀ 4.16E-08 TGI 1.11E-07 LC₅₀ 1.29E-05 SK-BR3 GI₅₀ 4.61E-09 TGI 1.27E-06 LC₅₀ 3.06E-07 K-562 GI₅₀ 1.72E-09 TGI 3.44E-09 LC₅₀ 5.94E-08 PANC-1 GI₅₀ 3.49E-09 TGI 1.01E-08 LC₅₀ 5.12E-07 LOVO GI₅₀ 5.07E-09 TGI 2.57E-08 LC₅₀ 4.19E-06 LOVO-DOX GI₅₀ 6.41E-08 TGI 7.00E-07 LC₅₀ 1.29E-05 HELA GI₅₀ TGI LC₅₀ HELA-APL GI₅₀ TGI LC₅₀ Toxicity Data

Toxicity was asssessed by the methods reported in Toxicology in Vitro, 15 (2001) 571-577, J. Luber Narod et al.: “Evaluation of the use of in vitro methodolodies as tools for screening new compounds for potential in vivo toxicity”.

Compound Liver Heart Myelo Skeletal Kidney 57 4.66E-09 3.48E-09 1.85E-08 REDO 3.35E-09 59 2.53E-08 8.14E-08 4.18E-08 1.46E-07 2.87E-08 61 1.32E-08 2.76E-08 1.69E-08 1.47E-08 5.12E-09 63 1.44E-08 6.66E-08 1.52E-08 3.06E-09 1.58E-08 64 2.57E-08 5.50E-08 1.93E-08 1.66E-09 1.77E-08 65 5.30E-09 9.00E-09 1.70E-08 3.77E-09 3.15E-09 67 3.20E-08 4.54E-08 3.27E-08 2.37E-08 5.36E-08 68 1.76E-08 1.13E-08 1.89E-08 1.27E-08 5.10E-09 70 3.16E-08 2.20E-07 6.61E-08 3.67E-08 1.07E-07 72 1.55E-08 3.78E-08 2.15E-08 1.32E-08 1.85E-08 74 3.07E-08 2.86E-08 3.30E-08 8.30E-10 3.05E-08 75 4.11E-08 8.17E-08 5.85E-08 4.06E-09 3.86E-08 76 1.35E-08 1.62E-08 8.19E-09 2.15E-09 3.20E-09 77 9.53E-09 1.64E-08 8.52E-09 2.20E-09 3.22E-09 78 5.88E-08 8.19E-07 NT 1.96E-08 2.59E-07 79 2.28E-08 3.46E-08 1.35E-08 2.75E-09 1.74E-08 86 1.47E-08 8.16E-08 8.35E-08 3.88E-08 1.37E-08 87 6.18E-08 3.60E-08 2.44E-07 2.00E-07 8.09E-08 92 2.30E-08 2.80E-08 1.92E-08 1.21E-08 1.35E-08 93 1.13E-08 4.46E-08 3.35E-09 5.52E-10 6.32E-08 94 1.24E-08 6.66E-08 1.13E-08 1.44E-09 3.49E-09 97 1.57E-08 9.63E-08 1.77E-08 4.62E-09 1.43E-08 98 4.21E-08 4.98E-08 3.79E-08 1.24E-08 1.08E-06 99 4.80E-08 1.13E-07 1.45E-07 9.71E-08 2.56E-08 101 5.40E-08 7.67E-08 1.96E-08 3.40E-09 3.17E-08 104 4.16E-09 3.44E-09 1.93E-08 4.10E-07 2.67E-09 161 8.58E-09 1.13E-08 2.27E-08 1.65E-08 2.60E-09 163 9.80E-07 4.80E-07 2.38E-07 2.53E-06 6.33E-07 165 1.68E-08 2.79E-08 2.87E-08 1.47E-08 1.89E-08 167 4.83E-07 4.28E-07 1.01E-06 1.09E-07 2.77E-07 170 3.58E-07 NT NT 3.29E-07 3.01E-07 171 8.37E-08 3.13E-08 1.37E-07 3.58E-08 2.70E-08 172 2.47E-07 7.52E-07 3.81E-07 8.53E-07 7.93E-07 173 4.03E-08 1.19E-07 4.98E-06 2.49E-06 7.09E-08 174 1.34E-08 2.76E-08 7.27E-08 9.80E-07 1.24E-08 175 3.87E-09 2.82E-09 1.59E-08 2.12E-07 2.84E-09 176 2.95E-08 1.98E-08 1.42E-08 2.41E-08 2.80E-09 182 3.98E-09 3.95E-08 3.19E-08 1.49E-08 1.26E-08 183 3.03E-08 3.72E-08 2.39E-08 2.67E-08 6.72E-03 212 8.68E-08 3.20E-08 8.58E-09 2.21E-08 3.34E-09 213 3.93E-08 1.82E-07 2.70E-08 1.72E-07 1.48E-08 217 1.07E-09 TT TT 3.37E-12 2.66E-13 

1. A compound of the general formula Ia:

wherein R₁, R₂, and R₅ are each independently selected from H, C(═O)R′, C(═O)OR′, P═O(OR′)₂, substituted or unsubstituted C₁-C₁₈ alkyl, substituted or unsubstituted C₂-C₁₈ alkenyl, substituted or unsubstituted C₂-C₁₈ alkynyl, substituted or unsubstituted C₆-C₁₈ carbocyclic aryl; wherein R₆ and R₇ are both ═O and the dotted lines indicate a quinone ring, or R₆ is —OR₃, where R₃ is H, C(═O)R′, C(═O)OR′, substituted or unsubstituted C₁-C₁₈ alkyl, substituted or unsubstituted C₂-C₁₈ alkenyl, substituted or unsubstituted C₂-C₁₈ alkynyl, substituted or unsubstituted C₆-C₁₈ carbocyclic aryl, R₇ is H, and the dotted lines indicate a phenyl ring; wherein X₂, X₃, X₄, X₅, X₆ are independently selected from H, OH, OR′, SH, SR′, SOR′, SO₂R′, C(═O)R′, C(═O)OR′, NO₂, NH₂, NHR′, N(R′)₂, NHC(O)R′, CN, halogen, unsubstituted C₁-C₂₄ alkyl, unsubstituted C₂-C₁₈ alkenyl, unsubstituted C₂-C₁₈ alkynyl, unsubstituted C₆-C₁₈ carbocyclic aryl, and unsubstituted heteroaromatic selected from coumarinyl, quinolinyl, pyridyl, pyrazinyl, pyrimidyl, furyl, pyrrolyl, thienyl, thiazolyl, oxazolyl, imidazolyl, indolyl, benzofuranyl, and benzothiazolyl; wherein X₁ is independently selected from OR₁, CN, (═O), or H; wherein when R₁, R₂, R₃, R₄, and R₅ are substituted, the substituents are each independently selected from the group consisting of OH, OR′, SH, SR′, SOR′, SO₂R′, C(═O)R′, C(═O)OR′, NO₂, NH₂, NHR′, N(R′)₂, NHC(O)R′, CN, halogen, ═O, unsubstituted C₁-C₁₈ alkyl, unsubstituted C₂-C₁₈ alkenyl, unsubstituted C₂-C₁₈ alkynyl, unsubstituted C₆-C₁₈ carbocyclic aryl, and unsubstituted heterocyclic selected from coumarinyl, quinolinyl, pyridyl, pyrazinyl, pyrimidyl, furyl, pyrrolyl, thienyl, thiazolyl, oxazolyl, imidazolyl, indolyl, benzofuranyl, benzothiazolyl, tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, morpholino and pyrrolindinyl; wherein each of the R′ groups is independently selected from the group consisting of H, OH, NO₂, NH₂, SH, CN, halogen, C(═O)H, C(═O)CH₃; CO₂H, PO(OR′)₂, substituted or unsubstituted C₁-C₁₈ alkyl, substituted or unsubstituted C₂-C₁₈ alkenyl, substituted or unsubstituted C₂-C₁₈ alkynyl, and substituted or unsubstituted C₆-C₁₈ carbocyclic aryl; wherein R₄ is selected from C(═O)R′, C(═O)OR′, P═O(OR′)₂, substituted or unsubstituted C₂-C₁₈ alkyl, substituted or unsubstituted C₂-C₁₈ alkenyl, substituted or unsubstituted C₂-C₁₈ alkynyl, and substituted or unsubstituted C₆-C₁₈ carbocyclic aryl; wherein when R₄ is C(═O)R′, C(═O)OR′, or P═O(OR′)₂, then each of the R′ groups is independently selected from the group consisting of H, OH, NO₂, NH₂, SH, CN, halogen, C(═O)H, C(═O)CH₃, CO₂H, PO(OR′)₂, substituted or unsubstituted C₂-C₁₈ alkyl, substituted or unsubstituted C₂-C₁₈ alkenyl, substituted or unsubstituted C₂-C₁₈ alkynyl, and unsubstituted C₆-C₁₈ carbocyclic aryl; and wherein when R′ is substituted, the substituents are each independently selected from the group consisting of halogen, cyano, hydroxyl, nitro, azido, unsubstituted C₁-C₆ alkanoyl, carboxamido, unsubstituted C₁-C₁₂ alkyl, unsubstituted C₂-C₁₂ alkenyl, unsubstituted C₂-C₁₂ alkynyl, unsubstituted C₁-C₁₂ alkoxy, unsubstituted C₆-C₁₈ carbocyclic aryloxy, unsubstituted C₁-C₁₂ alkylthio, unsubstituted C₁-C₁₂ alkylsulfinyl, unsubstituted C₁-C₁₂ alkylsulfonyl, unsubstituted C₁-C₁₂ aminoalkyl, unsubstituted C₆-C₁₈ carbocyclic aryl, unsubstituted aralkyl and unsubstituted heterocyclic group which is selected from coumarinyl, quinolinyl, pyridyl, pyrazinyl, pyrimidyl, furyl, pyrrolyl, thienyl, thiazolyl, oxazolyl, imidazolyl, indolyl, benzofuranyl, benzothiazolyl, tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, morpholino and pyrrolindinyl.
 2. A compound according to claim 1, wherein: R₆ is OR₃; R₁ and R₃ are independently selected from hydrogen, optionally substituted alkyl, optionally substituted alkenyl, C(═O)R′, or C(═O)OR′, where R′ is optionally substituted alkyl or optionally substituted alkenyl, the optional substituents being chosen from halo, amino, amino derived from amino acid, unsubstituted C₆-C₁₈ carbocyclic aryl or unsubstituted heterocyclic, which is selected from coumarinyl, quinolinyl, pyridyl, pyrazinyl, pyrimidyl, furyl, pyrrolyl, thienyl, thiazolyl, oxazolyl, imidazolyl, indolyl, benzofuranyl, benzothiazolyl, tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, morpholino and pyrrolindinyl; R₂ is hydrogen, alkyl or C(═O)OR′, where R′ is alkyl; R₅ is hydrogen, alkyl or C(═O)OR′, where R′ is alkenyl; X₁ is hydrogen, hydroxy, or cyano; X₂, X₄ and X₅ are hydrogen; X₃ is OR′, where R′ is alkyl; X₆ is hydrogen or unsubstituted alkyl; R₇ is hydrogen; and the dotted lines indicate a phenyl ring.
 3. A compound according to claim 1, wherein R₁ is: hydrogen; alkyl; C(═O)R′, where R′ is optionally substituted alkyl, optionally substituted haloalkyl, optionally substituted heterocyclicalkyl, optionally substituted aminoalkyl, optionally substituted arylalkenyl, optionally substituted alkenyl, optionally substituted aralkyl; or C(═O)OR′, where R′ is alkyl or alkenyl.
 4. A compound according to claim 1, wherein R₂ is hydrogen, methyl, or alkoxycarbonyl.
 5. A compound according to claim 1, wherein R₃ is: hydrogen; alkyl; (C═O)R′, where R′ is optionally substituted alkyl, optionally substituted haloalkyl, optionally substituted arylalkenyl, optionally substituted heterocyclicalkyl, optionally substituted alkenyl, optionally substituted aralkyl; or (C═O)OR′, where R′ is alkyl, alkenyl, or aralkyl.
 6. A compound according to claim 1,. wherein R₄ is: C(═O)R′, where R′ is optionally substituted alkyl, optionally substituted haloalkyl, optionally substituted aralkyl, optionally substituted arylalkenyl, optionally substituted aminoalkyl, optionally substituted heterocyclicalkyl; or (C═O)OR′, where R′ is alkyl, alkenyl, or aralkyl.
 7. A compound according to claim 1, wherein R₅ is: hydrogen; alkyl; (C═O)OR′, where R′ is alkenyl.
 8. A compound according to claim 1, wherein X₁ is hydrogen, hydroxy, or cyano.
 9. A compound according to claim 1, wherein X₂ is hydrogen.
 10. A compound according to claim 1, wherein X₃ is OR′, where R′ is alkyl.
 11. A compound according to claim 1, wherein X₄ is hydrogen.
 12. A compound according to claim 1 ,wherein X₅ is hydrogen.
 13. A compound according to claim 1, wherein X₆ is hydrogen or alkyl.
 14. A compound according to claim 1, wherein R₁ is C(═O)R′, where R′ is optionally substituted alkyl with at least 4 carbon atoms or optionally substituted alkenyl.
 15. A compound according to claim 14, wherein the optional substituent of R₁ is unsubstituted C₆-C₁₈ carbocyclic aryl or unsubstituted heterocyclic, which is selected from coumarinyl, quinolinyl, pyridyl, pyrazinyl, pyrimidyl, furyl, pyrrolyl, thienyl, thiazolyl, oxazolyl, imidazolyl, indolyl, benzofuranyl, benzothiazolyl, tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, morpholino and pyrrolindinyl, or R′ is derived from an optionally protected amino acid.
 16. A compound according to claim 1, wherein R₃ is: hydrogen; C₁-C₆ alkyl; cinnamoyl; (C═O)R′ where R′ is C₁-C₁₈ alkyl, perfluoroC₁-C₄ alkyl, heterocyclicalkyl containing an alkyl of 1 to 6 carbon atoms with a unsubstituted ω-heterocyclic substituent which is selected from coumarinyl, quinolinyl, pyridyl, pyrazinyl, pyrimidyl, furyl, pyrrolyl, thienyl, thiazolyl, oxazolyl, imidazolyl, indolyl, benzofuranyl, benzothiazolyl, tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, morpholino and pyrrolindinyl, allyl, or benzyl; or (C═O)OR′ where R′ is C₁-C₆ alkyl, vinyl, allyl, or benzyl.
 17. A compound according to claim 1, wherein R₄ is: unsubstituted cinnamoyl; or (C═)R′, where R′ is C₁₂-C₁₈ alkyl, ω-chloro- or perfluoro- C₂-C₄ alkyl, phenethyl, aminoacid, heterocyclicalkyl containing an alkyl of 2 to 6 carbon atoms with a unsubstituted ω-heterocyclic substituent which is selected from coumarinyl, quinolinyl, pyridyl, pyrazinyl, pyrimidyl, furyl, pyrrolyl, thienyl, thiazolyl, oxazolyl, imidazolyl, indolyl, benzofuranyl, benzothiazolyl, tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, morpholino and pyrrolindinyl; or (C═O)OR′, where R′ is C₂-C₆ alkyl, vinyl, or allyl.
 18. A pharmaceutical composition comprising a compound according to claim 1, and a pharmaceutical carrier.
 19. A method of treating lung cancer, colon cancer, kidney cancer, prostate cancer, ovarian cancer, breast cancer, pancreas cancer, leukaemia or melanoma in a subject, which comprises administering to the subject a compound according to claim
 1. 20. A compound according to claim 1 of formula: 